

 
COVID-19 and Access to Medical Products: 
Implications of Section 301 Tariffs 
Updated February 16, 2022 
Congressional Research Service 
https://crsreports.congress.gov 
R46954 
 
  
 
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COVID-19 and Access to Medical Products: Implications of Section 301 Tariffs 
 
Contents 
Overview ......................................................................................................................................... 1 
Background on Section 301 Tariffs ................................................................................................. 2 
Reinstating Previously Extended Tariff Exclusions ........................................................................ 3 
Medical-Care and COVID-19 Response Products .......................................................................... 4 
Outlook ............................................................................................................................................ 4 
 
Tables 
Table 1. Section 301 Tariff Exclusion Extensions Granted and Under Review: Medical-
Care and COVID-19 Response Products ..................................................................................... 4 
Table 2. Section 301 Tariff Exclusion Extensions Under Review: Other Products With 
Potential Uses For COVID-19 Response Efforts ....................................................................... 14 
  
Contacts 
Author Information ........................................................................................................................ 16 
 
 
  
COVID-19 and Access to Medical Products: Implications of Section 301 Tariffs 
 
Overview 
On October 8, 2021, the Office of the U.S. Trade Representative (USTR) published a Federal 
Register notice seeking comments on whether to reopen the process by which U.S. stakeholders 
could apply for exclusions from Section 301 tariffs on U.S. imports from China.1 Specifically, the 
agency requested comments on whether to reinstate 549 exclusions that were previously extended 
and had expired or were set to expire soon.2 Some of these exclusions cover products with known 
or potential medical uses related to the U.S. response to the Coronavirus Disease 2019 (COVID-
19) pandemic. The USTR collected comments through its portal until December 1, 2021. 
Separately, in light of the spread of the COVID-19 Delta variant last summer and developments 
in the production capacity of U.S.-based manufacturers to satisfy various national needs, the 
USTR concluded a review of public comments on whether 99 exclusions on medical-care and/or 
COVID-19 response products needed to be further extended for six months (“COVID-19 
Review”).3 In response to these comments and the advice from advisory committees, the 
interagency Section 301 Committee, and the White House COVID-19 Response Team, the USTR 
determined on November 9, 2021, to provide a transition period for all COVID-19 exclusions set 
to expire on November 14 (through November 30) and to extend 81 of the 99 COVID-19 
exclusions through May 31, 2022.4 Eighty of the 99 exclusions also could potentially be 
reinstated or further extended beyond May 2022 under the ongoing review process announced in 
October (“General Review”).5 The agency clarified that the criteria used for granting exclusions 
under the general review will be different than that applied under the COVID-19 review, and that 
it may result in different effective dates for any exclusions granted.6 
Some Members of Congress have raised concerns about the exclusion process.7 They have 
questioned USTR’s ability to “pick winners and losers” through granting or denying requests or 
have pushed for broad tariff relief amid concerns about the negative impact of tariffs on the U.S. 
economy. This has been the case particularly in the aftermath of the COVID-19 pandemic, which 
                                                 
1 Office of the U.S. Trade Representative, “Request for Comments on the Possible Reinstatement of Certain Exclusions 
in the Section 301 Investigation of China’s Acts, Policies, and Practices Related to Technology Transfer, Intellectual 
Property, and Innovation,” 86 FR 56345, October 8, 2021. 
2 For more detail, see Office of the U.S. Trade Representative, “Index of 549 Previously Extended Exclusions.” 
3 The time window to submit comments on particular COVID-19 exclusions (“COVID-19 Review”) opened on August 
27 and closed on September 27, 2021. Office of the U.S. Trade Representative, “Request for Comments on Certain 
Products Exclusions Related to COVID-19: China’s Acts, Policies, and Practices Related to Technology Transfer, 
Intellectual Property, and Innovation,” 86 FR 48280, August 27, 2021. The 99 COVID-19 exclusions were originally 
scheduled to expire on September 30 but were temporarily extended through November 14, 2021, as the review 
continued. Office of the U.S. Trade Representative, “Notice of Product Exclusion Extensions: China’s Acts, Policies, 
and Practices Related to Technology Transfer, Intellectual Property, and Innovation,” 86 FR 54011, September 29, 
2021. 
4 Office of the U.S. Trade Representative, “Notice of Product Exclusion Extensions: China’s Acts, Policies, and 
Practices Related to Technology Transfer, Intellectual Property, and Innovation,” 86 FR 63438, November 16, 2021. 
5 The time window to submit comments on the reinstatement of exclusions (“General Review”) opened on October 12 
and is set to close on December 1, 2021. 
6 Office of the U.S. Trade Representative, “Guidance Regarding Products Covered Both in the COVID Exclusion 
Notices and the Notices Concerning Possible Reinstatement of Previously Extended Exclusions.” 
7 For example, Senators Ron Wyden and Thomas R. Carper, from the U.S. Senate Committee on Finance, and Senator 
Tim Kaine asked the U.S. Government Accountability Office (GAO) to review how the USTR decided to exclude 
products from China from tariffs under Section 301. For more detail, see GAO’s report, “U.S.-China Trade: USTR 
Should Fully Document Internal Procedures for Making Tariff Exclusion and Extension Decisions,” GAO-21-506, July 
28, 2021. 
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COVID-19 and Access to Medical Products: Implications of Section 301 Tariffs 
 
has affected the United States’ ability to obtain certain products domestically or from countries 
other than China. Other Members oppose granting any exclusions on the ground that doing so 
may undermine Section 301’s effectiveness at addressing China’s unfair trade practices or hinder 
U.S. efforts to incentivize domestic manufacturing of certain critical goods. The USTR’s 2021 
actions were not aimed at providing broader tariff relief. They were limited to extending 
unexpired exclusions on medical supplies relevant to combatting the COVID-19 pandemic and 
requesting comments on whether to reinstate exclusions that were previously extended.8 
This report provides a brief overview of the “General Review” as it pertains to medical products. 
It also includes a list of relevant exclusions categorized by: Harmonized Tariff Schedule of the 
United States (HTS) subheading, type (entire subheading or product specific), round/action (Lists 
1 through 4A), expiration date, and review process (COVID-19, General, or both). For more 
detail about Section 301, see CRS Report R46604, Section 301 of the Trade Act of 1974: Origin, 
Evolution, and Use. 
Background on Section 301 Tariffs 
In 2018, the USTR determined, pursuant to an investigation under “Section 301” (Title III of the 
Trade Act of 1974, 19 U.S.C. §§2411-2420), that China’s acts, policies, and practices related to 
technology transfer, intellectual property (IP), and innovation were unreasonable or 
discriminatory and burdened or restricted U.S. commerce. In an effort to counter these policies 
and obtain their elimination, the Trump Administration imposed, under Section 301, four rounds 
(Lists 1 through 4A) of increased tariffs on about two-thirds of U.S. imports from China. 
However, in an effort to mitigate harm to U.S. interests, the USTR created a process whereby 
interested parties could request that a particular product be excluded from the tariffs, subject to 
certain criteria. Title III of the Trade Act of 1974 does not outline a formal process for exclusions 
or require the USTR to establish one. The determination to do so appears to be solely at the 
USTR’s discretion. 
Overview of Section 301 
Title III of the Trade Act of 1974 (Sections 301-310, codified at 19 U.S.C. §§2411-2420), titled “Relief from Unfair 
Trade Practices," is col ectively referred to as "Section 301." It grants the USTR a range of responsibilities and 
authorities to impose trade sanctions on foreign countries that violate U.S. trade agreements or engage in acts 
that are "unjustifiable," "unreasonable," or "discriminatory" and burden U.S. commerce. Prior to 1995, the United 
States used Section 301 to unilaterally pressure other countries to eliminate trade barriers and open their markets 
to U.S. exports. The creation of an enforceable dispute settlement mechanism in the World Trade Organization 
(WTO), strongly supported by the United States at the time, significantly reduced the use of Section 301. While 
the United States retains the flexibility to seek recourse for foreign unfair trade practices in the WTO or under 
Section 301, a determination to bypass WTO dispute settlement and impose retaliatory measures in response to a 
Section 301 investigation may be challenged at the WTO.  
Since 2017, the USTR has launched Section 301 investigations against China, the European Union (EU), France, a 
group of 10 trading partners, and Vietnam. Two investigations have resulted in the USTR imposing tariffs to date: 
on U.S. imports from China and the EU. The U.S. action against the EU—unlike that against China—was based on 
a WTO dispute in which the USTR anticipated being allowed to retaliate. 
                                                 
8 In March 2021, the USTR extended—through September 2021—the 99 exclusions granted or extended in December 
2020. To provide time to review comments received between August and September 2021, the USTR adopted an 
interim 45-day extension of the exclusions that were set to expire on September 30 through November 14, 2021. Office 
of the U.S. Trade Representative, “Notice of Product Exclusion Extensions: China’s Acts, Policies, and Practices 
Related to Technology Transfer, Intellectual Property, and Innovation,” 86 FR 13785, March 10, 2021, and “Notice of 
Product Exclusion Extensions: China’s Acts, Policies, and Practices Related to Technology Transfer, Intellectual 
Property, and Innovation,” 86 FR 54011, September 29, 2021. 
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COVID-19 and Access to Medical Products: Implications of Section 301 Tariffs 
 
For more detail, see CRS In Focus IF11346, Section 301 of the Trade Act of 1974 and CRS Report R46604, Section 
301 of the Trade Act of 1974: Origin, Evolution, and Use. 
Reinstating Previously Extended Tariff Exclusions 
Under the comment period and review announced in October 2021, importers and interested 
parties—including law firms and trade associations—could submit comments through December 
1, supporting (or opposing) the reinstatement of a specific exclusion extension, including for how 
long it should be reinstated. The 549 exclusions eligible for reinstatement are reflected in 563 
specially prepared product descriptions (“specific products”) or 10-digit HTS subheading 
(“product categories”). Parties were not able to petition the USTR for new exclusions or 
extensions to expired exclusions that were not previously extended. 
The USTR indicated that it will evaluate each extension request on a case-by-case basis, taking 
into account the following: (1) availability of the product in question from non-Chinese sources; 
(2) attempts by the importer to source the product from the United States or third countries; (3) 
the potential impact that further extensions could have in countering or eliminating China’s trade 
practices covered in the Section 301 investigation; and (4) the extent to which the imposition of 
Section 301 tariffs on the particular product will cause severe economic harm to the commenter 
or other U.S. interests, including small businesses, employment, manufacturing output, and 
critical supply chains in the United States.9 
The USTR did not announce a timetable for providing responses to filed comments. However, the 
agency indicated that it will publish decisions on reinstated exclusions through Federal Register 
notices and that the exclusions will be retroactive to October 12, 2021. Exclusions apply 
generally to specified products, so any party importing a product covered by a reinstated 
exclusion may file a claim. Importers whose goods entered or were withdrawn from warehouse 
for consumption on or after October 12, 2021, may request tariff refunds from U.S. Customs and 
Border Protection (CBP), provided that CBP has not already calculated the final duties owed by 
the time the importers file the refund claim (see text box). 
Retroactive Section 301 Tariff Exclusions 
Section 301 product exclusions granted by the U.S. Trade Representative (USTR) “may be retroactive for 
unliquidated entries and for entries that are liquidated but where the liquidation is not final and the protest period 
has not expired. 
If a product exclusion has been granted, an importer of record (IOR) may request a refund by filing a corrective 
action with CBP by filing a post summary correction (PSC) for unliquidated entries or file a protest for entries that 
have liquidated but where the liquidation is not final and the protest period has not expired. 
When a product exclusion is granted, an importer may submit a PSC to request a refund on unliquidated entries 
up to 15 days prior to the scheduled liquidation date (generally within 300 days from the date of entry summary 
filing). If an entry summary is set to liquidate in less than 15 days or has already liquidated, the entry summary is 
beyond the PSC filing period. However, the importer may file a protest so long as the protest is filed within the 
180-day period fol owing liquidation of the impacted entry summary(ies).” 
Source: U.S. Customs and Border Protection, “CSMS #42566154: Section 232 and Section 301–Extensions Requests, PSCs, 
and Protests,” May 1, 2020. 
                                                 
9 Office of the U.S. Trade Representative, “Request for Comments on the Possible Reinstatement of Certain Exclusions 
in the Section 301 Investigation of China’s Acts, Policies, and Practices Related to Technology Transfer, Intellectual 
Property, and Innovation,” 86 FR 56345, October 8, 2021. 
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Medical-Care and COVID-19 Response Products 
Of the 549 exclusion extensions eligible for reinstatement, CRS was able to identify 23 product 
categories and 64 specific products with known medical uses (Table 1). Other exclusions eligible 
for reinstatement—but not formally identified by the USTR as medical or COVID-related—may 
apply to products that have potential medical uses, can serve as inputs for the manufacture of 
medical products, or can be used in pandemic response efforts (see, for example, Table 2). 
However, their ultimate purpose may not always be easily ascertained from HTS subheadings or 
product descriptions (e.g., organic chemicals or textiles for the manufacture of pharmaceuticals or 
personal protective equipment). 
Outlook 
In recent years, some Members have introduced legislation to amend Title III of the Trade Act of 
1974, while also raising the issue of establishing or streamlining an exclusion process during 
hearings and in letters to the USTR. For example, the United States Innovation and Competition 
Act of 2021 (S. 1260), if enacted, would suspend tariffs—including those imposed under Section 
301—on certain goods needed to combat the COVID-19 pandemic and would set out a process 
for excluding imports from Section 301 tariffs in statute, rather than allow USTR to create its 
own process.  
The Biden Administration continues to review its trade strategy for China, thus far announcing 
potential renewal of the Section 301 tariff exclusion process and focusing on enforcement of the 
U.S.-China “Phase One” trade agreement.10 It is possible that the Biden Administration could use 
Section 301 authorities to counter or obtain the elimination of other Chinese practices that may 
disadvantage or discriminate against U.S. exports, firms, and workers in the future.  
Congress may wish to engage with the Administration to develop and implement specific 
guidelines for when and how to grant and extend exclusions. This has the potential to promote 
transparency, consistency, and proper application of standards in reviewing exclusion requests, 
thereby helping to ensure that the USTR carries out Section 301 objectives as prescribed by 
Congress. 
Table 1. Section 301 Tariff Exclusion Extensions Granted and Under Review: Medical-
Care and COVID-19 Response Products 
Type of 
Subheading or Product 
Expiration 
HTS Code 
Exclusion 
Description 
List 
Date 
Review 
2805.11.0000  Product 
Sodium metal (CAS No. 7440-23-5), in 
3 
05/31/2022 
COVID-19 & 
Specific 
bulk solid form 
General 
3401.19.0000  Entire 
Soap & other organic surface-active 
4A 
05/31/2022 
COVID-19 & 
Subheading  products, not for toilet use, in bars, 
General 
cakes, molded pieces, and paper, etc. 
impregnated or coated with soap or 
detergent 
                                                 
10 Office of the U.S. Trade Representative, “Fact Sheet: The Biden-Harris Administration’s New Approach to the U.S.-
China Trade Relationship,” Press Release, October 4, 2021. 
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COVID-19 and Access to Medical Products: Implications of Section 301 Tariffs 
 
Type of 
Subheading or Product 
Expiration 
HTS Code 
Exclusion 
Description 
List 
Date 
Review 
3401.30.5000  Product 
Hand soaps and hand sanitizers in the 
3 
11/30/2021 
COVID-19 
Specific 
form of liquid or cream put up for 
retail sale, other than hand sanitizers of 
heading 3808 
3401.30.5000  Product 
Disposable cloths of nonwoven textile 
3 
05/31/2022 
COVID-19 & 
Specific 
materials impregnated, coated or 
General 
covered with organic surface-active 
preparations for washing the skin, put 
up for retail sale 
3401.30.5000  Product 
Organic surface-active liquid for 
3 
11/30/2021 
COVID-19 & 
Specific 
washing the skin, not containing any 
General 
aromatic or modified aromatic surface-
active agent, put up for retail sale in a 
bottle of plastics with pump-action top, 
each bottle measuring not more than 
17 cm in width, not more than 27 cm 
in height and not more than 6.5 cm in 
length and with a net weight of not 
more than 0.5 kg  
3808.94.1000  Entire 
Disinfectants containing any aromatic 
3 
05/31/2022 
COVID-19 
Subheading  or modified aromatic disinfectant 
3808.94.5010  Entire 
Wipes impregnated with alcohol or 
3 
05/31/2022 
COVID-19 
Subheading  other disinfectants, other than paper 
wipes or nonwoven wipes 
3808.94.5050  Entire 
Hydrogen peroxide put up in 
3 
11/30/2021 
COVID-19 
Subheading  disinfectant preparations for sanitizing 
or disinfecting surfaces 
3808.94.5080  Entire 
Alcohol-based hand sanitizer 
3 
11/30/2021 
COVID-19 
Subheading  containing 60% or more by weight of 
ethanol, of a kind described in 
statistical note 1 to Chapter 38 
3808.94.5095  Entire 
Disinfectants, NESOI (described in 
3 
11/30/2021 
COVID-19 
Subheading  statistical reporting number 
3808.94.5090 prior to July 1, 2021) 
3824.99.9297  Product 
Silicon monoxide in powder form 
3 
05/31/2022 
COVID-19 & 
Specific 
General 
3824.99.9297  Product 
Mixtures containing 
3 
05/31/2022 
COVID-19 & 
Specific 
N,Ndimethyldodecan-1-amine (CAS 
General 
No. 112-18-5) and N,N-
dimethyltetradecan-1-amine (CAS No. 
112-75-4) [*] 
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COVID-19 and Access to Medical Products: Implications of Section 301 Tariffs 
 
Type of 
Subheading or Product 
Expiration 
HTS Code 
Exclusion 
Description 
List 
Date 
Review 
3917.29.0090  Product 
Molded acrylonitrile-butadiene-styrene 
2 
05/31/2022 
COVID-19 & 
Specific 
tubes, of a kind used to effect the 
General 
sterile transfer of fluid from a bag or 
vial to another container, each tube 
measuring 7.5 cm or more but not 
exceeding 23 cm in length, with an 
inner diameter of less than 0.65 cm 
and an outer diameter of less than 9 
cm, one end having been angle-cut to 
form a spike, and having an integrated 
flange, less than 3 cm in diameter near 
the spike end and removable 
polyethylene caps on each end, put up 
in sterile packing 
3917.33.0000  Product 
Flexible oxygen tubes, pipes and hoses 
3 
05/31/2022 
COVID-19 
Specific 
presented with integrated molded 
connectors, of polyvinyl chloride 
3917.33.0000  Product 
Flexible gas sampling tubes, pipes and 
3 
05/31/2022 
COVID-19 
Specific 
hoses, of polyvinyl chloride, with lock 
connectors at each end  
3919.90.5060  Product 
Polyethylene film, 20.32 to 198.12 cm 
2 
11/30/2021 
COVID-19 & 
Specific 
in width, and 30.5 to 2000.5 m in 
General 
length, coated on one side with solvent 
acrylic adhesive, clear or in transparent 
colors, whether or not printed, in rol s 
3920.10.0000  Product 
Rectangular sheets of high-density or 
2 
05/31/2022 
COVID-19 & 
Specific 
low-density polyethylene, 111.75 cm to 
General 
215.9 cm in width, and 152.4 cm to 
304.8 cm in length, with a sticker 
attached to mark the center of each 
sheet, of a kind used in hospital or 
surgery center operating rooms  
3921.19.0000  Product 
Sheets and strips consisting of both 
2 
05/31/2022 
COVID-19 & 
Specific 
cross-linked polyethylene and ethylene 
General 
vinyl acetate, of a width greater than 1 
m but not greater than 1.5 m, and a 
length greater than 1.75 m but not 
greater than 2.6 m 
3921.90.1500  Product 
Polyethylene sheet and film laminated 
2 
05/31/2022 
COVID-19 & 
Specific 
with spunbond-spunbond-spunbond 
General 
nonwoven polypropylene fabric, 
measuring 1.12 m or more but not 
over 1.52 m in width and 1.93 m or 
more but not over 2.29 m in length, 
and weighing 55 g/m² or more but not 
exceeding 88 g/m² 
3923.10.9000  Product 
Container units of plastics, each 
3 
05/31/2022 
COVID-19 & 
Specific 
comprising a tub and lid therefore, 
General 
configured or fitted for the 
conveyance, packing, or dispensing of 
wet wipes 
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Type of 
Subheading or Product 
Expiration 
HTS Code 
Exclusion 
Description 
List 
Date 
Review 
3923.21.0030  Product 
Sacks and bags of polymers of 
3 
05/31/2022 
COVID-19 
Specific 
ethylene, reclosable, qualifying as Class 
1 medical devices by the U.S. Food and 
Drug Administration under product 
code NNI 
3923.21.0095  Entire 
Sacks and bags of polymers of 
3 
05/31/2022 
COVID-19 & 
Subheading  ethylene, NESOI 
General 
3923.50.0000  Product 
Injection molded polypropylene plastic 
3 
05/31/2022 
COVID-19 & 
Specific 
caps or lids each weighing not over 24 
General 
grams designed for dispensing wet 
wipes 
3926.20.9010  Product 
Aprons, of plastic, of a kind used as 
3 
11/30/2021 
COVID-19 
Specific 
personal protective equipment 
3926.20.9050  Entire 
Articles of apparel & clothing 
3 
05/31/2022 
COVID-19 & 
Subheading  accessories, of plastic, NESOI 
General 
3926.90.9910  Entire 
Laboratory ware 
4A 
05/31/2022 
COVID-19 & 
Subheading 
General 
3926.90.9950  Product 
Face shields of transparent plastics, 
4A 
05/31/2022 
COVID-19 
Specific 
whether or not assembled 
3926.90.9985  Product 
Bowls of molded plastics, with clips for 
4A 
05/31/2022 
COVID-19 & 
Specific 
retaining guide wires during surgical 
General 
procedures (described in statistical 
reporting number 3926.90.9990 prior 
to July 1, 2020) 
3926.90.9985  Product 
Disposable graduated medicine 
4A 
05/31/2022 
COVID-19 & 
Specific 
dispensing cups of plastics (described 
General 
in statistical reporting number 
3926.90.9990 prior to July 1, 2020) 
3926.90.9985  Product 
Single-use sterile drapes and covers of 
4A 
05/31/2022 
COVID-19 & 
Specific 
plastics, of a kind used to protect the 
General 
sterile field in surgical operating rooms 
(described in statistical reporting 
number 3926.90.9990 prior to July 1, 
2020) 
3926.90.9985  Product 
Sterile decanters of polystyrene 
4A 
05/31/2022 
COVID-19 & 
Specific 
plastics, each of a kind used to transfer 
General 
aseptic fluids or medication to and 
from sterile bags, vials or glass 
containers (described in statistical 
reporting number 3926.90.9990 prior 
to July 1, 2020) 
3926.90.9985  Product 
Coverings, of plastics, designed to fit 
4A 
05/31/2022 
COVID-19 & 
Specific 
over wound sites or casts thereby 
General 
forming a protective seal for keeping 
the covered area dry and debris free 
while showering or bathing (described 
in statistical reporting number 
3926.90.9990 prior to July 1, 2020) 
4015.19.0510  Entire 
Medical gloves, mittens and mitts of 
4A 
11/30/2021 
COVID-19 & 
Subheading  natural rubber, other than hard rubber 
General 
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Type of 
Subheading or Product 
Expiration 
HTS Code 
Exclusion 
Description 
List 
Date 
Review 
4015.19.0550  Entire 
Medical gloves, of vulcanized rubber 
4A 
11/30/2021 
COVID-19 & 
Subheading  other than hard rubber, NESOI 
General 
4015.19.1010  Entire 
Seamless, disposable gloves, of 
3 
11/30/2021 
COVID-19 & 
Subheading  vulcanized rubber other than hard 
General 
rubber 
4015.19.1010  Product 
Seamless disposable gloves of 
3 
11/30/2021 
COVID-19 & 
Specific 
acrylonitrile butadiene rubber, other 
General 
than for surgical or medical use 
4015.19.1010  Product 
Seamless disposable gloves of natural 
3 
11/30/2021 
COVID-19 & 
Specific 
rubber latex, other than for surgical or 
General 
medical use 
4818.90.0020  Entire 
Face masks of paper pulp, paper 
4A 
05/31/2022 
COVID-19 & 
Subheading  cellulose wadding or webs of cellulose 
General 
fibers 
4818.90.0080  Entire 
Bed sheets and similar household or 
4A 
05/31/2022 
COVID-19 & 
Subheading  hospital articles of paper pulp, paper 
General 
cellulose wadding or webs of cellulose 
fibers, NESOI 
4819.50.4060  Entire 
Packing containers, NESOI, of paper, 
3 
05/31/2022 
COVID-19 & 
Subheading  paperboard, cellulose wadding or webs 
General 
of cellulose fibers 
5210.11.4040  Entire 
Woven fabrics of cotton, containing 
4A 
05/31/2022 
COVID-19 & 
Subheading  less than 85 percent by weight of 
General 
cotton, mixed mainly or solely with 
man-made fibers, weighing not more 
than 200 g/m2, unbleached, Plain 
Weave, of number 42 or lower 
number, sheeting 
5210.11.6020  Entire 
Woven fabrics of cotton, containing 
4A 
05/31/2022 
COVID-19 & 
Subheading  less than 85 percent by weight of 
General 
cotton, mixed mainly or solely with 
man-made fibers, weighing not more 
than 200 g/m2, unbleached, plain 
weave, of numbers 43 to 68, poplin or 
broadcloth 
5504.10.0000  Entire 
Artificial staple fibers, not carded, 
3 
05/31/2022 
COVID-19 & 
Subheading  combed or otherwise processed for 
General 
spinning: of viscose rayon 
5603.12.0090  Entire 
Nonwovens, whether or not 
3 
05/31/2022 
COVID-19 & 
Subheading  impregnated, coated, covered or 
General 
laminated, of man-made filaments, 
weighing more than 25 g/m2 but not 
more than 70 g/m2, other 
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COVID-19 and Access to Medical Products: Implications of Section 301 Tariffs 
 
Type of 
Subheading or Product 
Expiration 
HTS Code 
Exclusion 
Description 
List 
Date 
Review 
5603.12.0090  Product 
Nonwoven fabrics of man-made fibers, 
3 
11/30/2021 
COVID-19 & 
Specific 
weighing more than 25 g/m2 but not 
General 
more than 70 g/m2, with a smooth or 
embossed texture (not impregnated, 
coated or covered with material other 
than or in addition to rubber, plastics, 
wood pulp or glass fibers), in rol s that 
are pre-slitted in lengths of not less 
than 15 cm to not more than 107 cm, 
for use in the manufacture of personal 
care wipes 
5603.14.9090  Entire 
Other nonwovens, whether or not 
3 
05/31/2022 
COVID-19 & 
Subheading  impregnated, coated, covered or 
General 
laminated, of man-made filaments, 
weighing more than 150 g/m2, other 
than laminated fabrics, not 
impregnated, coated or covered with 
material other than or in addition to 
rubber, plastics, wood pulp or glass 
fibers 
5603.92.0090  Entire 
Other non-woven fabrics, not man-
3 
05/31/2022 
COVID-19 & 
Subheading  made, other than floor covering 
General 
underlays & laminated fabrics, not 
impregnated, coated, or covered, 
weighing more than 25 g/m2 and less 
than 70 g/m2 
5603.93.0090  Entire 
Other non-woven fabrics, not man-
3 
05/31/2022 
COVID-19 & 
Subheading  made, other than floor covering 
General 
underlays & laminated fabrics, not 
impregnated, covered, weighing more 
than 70 g/m2 and less than 150 g/m2 
6116.10.6500  Product 
Gloves, containing less than 50% by 
3 
11/30/2021 
COVID-19 & 
Specific 
weight of textile fibers, coated with 
General 
rubber or plastics designed for 
enhanced grip 
6210.10.5010  Entire 
Surgical or isolation gowns, disposable, 
4A 
05/31/2022 
COVID-19 & 
Subheading  of nonwoven fabrics of heading 5602 
General 
or 5603 
6210.10.5090  Entire 
Disposable apparel designed for use in 
4A 
05/31/2022 
COVID-19 & 
Subheading  hospitals, clinics, laboratories and 
General 
other areas, of nonwoven fabrics of 
heading 5602 or 5603, NESOI 
6307.90.6090  Entire 
Other made up articles, including dress  4A 
11/30/2021 
COVID-19 & 
Subheading  patterns: surgical drapes, of fabric 
General 
formed on a base of paper or covered 
with paper, other 
6307.90.6800  Entire 
Other made up articles, including dress  4A 
11/30/2021 
COVID-19 & 
Subheading  patterns: surgical drapes of spun laced 
General 
or bonded fiber fabric disposable 
surgical drapes of man-made fibers 
Congressional Research Service  
 
9 
COVID-19 and Access to Medical Products: Implications of Section 301 Tariffs 
 
Type of 
Subheading or Product 
Expiration 
HTS Code 
Exclusion 
Description 
List 
Date 
Review 
6307.90.7200  Entire 
Other made up articles, including dress  4A 
05/31/2022 
COVID-19 
Subheading  patterns: surgical drapes, NESOI, not 
spun laced or bonded fiber fabric. 
6307.90.9845  Product 
Face masks and particulate facepiece 
4A 
11/30/2021 
COVID-19 & 
Specific 
respirators, of textile fabrics 
General 
(described in statistical reporting 
number 6307.90.9889 prior to July 1, 
2020) 
6307.90.9845  Product 
Single-use medical masks of textile 
4A 
11/30/2021 
COVID-19 & 
Specific 
material (described in statistical 
General 
reporting number 6307.90.9889 prior 
to July 1, 2020) 
6307.90.9850  Product 
Face masks and particulate facepiece 
4A 
11/30/2021 
COVID-19 & 
Specific 
respirators, of textile fabrics 
General 
(described in statistical reporting 
number 6307.90.9889 prior to July 1, 
2020) 
6307.90.9850  Product 
Single-use medical masks of textile 
4A 
11/30/2021 
COVID-19 & 
Specific 
material (described in statistical 
General 
reporting number 6307.90.9889 prior 
to July 1, 2020) 
6307.90.9870  Product 
Face masks and particulate facepiece 
4A 
11/30/2021 
COVID-19 & 
Specific 
respirators, of textile fabrics 
General 
(described in statistical reporting 
number 6307.90.9889 prior to July 1, 
2020) 
6307.90.9870  Product 
Single-use medical masks of textile 
4A 
11/30/2021 
COVID-19 & 
Specific 
material (described in statistical 
General 
reporting number 6307.90.9889 prior 
to July 1, 2020) 
6307.90.9875  Product 
Face masks and particulate facepiece 
4A 
11/30/2021 
COVID-19 & 
Specific 
respirators, of textile fabrics 
General 
(described in statistical reporting 
number 6307.90.9889 prior to July 1, 
2020) 
6307.90.9891  Product 
Cold packs consisting of a single-use, 
4A 
05/31/2022 
COVID-19 & 
Specific 
instant, endothermic chemical reaction 
General 
cold pack combined with a textile 
exterior lining (described in statistical 
reporting number 6307.90.9889 prior 
to July 1, 2020) 
6307.90.9891  Product 
Disposable shoe and boot covers of 
4A 
11/30/2021 
COVID-19 & 
Specific 
man-made fiber fabrics (described in 
General 
statistical reporting number 
6307.90.9889 prior to July 1, 2020) 
6307.90.9891  Product 
Hot packs of textile material, single-
4A 
05/31/2022 
COVID-19 & 
Specific 
use (described in statistical reporting 
General 
number 6307.90.9889 prior to July 1, 
2020) 
Congressional Research Service  
 
10 
COVID-19 and Access to Medical Products: Implications of Section 301 Tariffs 
 
Type of 
Subheading or Product 
Expiration 
HTS Code 
Exclusion 
Description 
List 
Date 
Review 
6307.90.9891  Product 
Laparotomy sponges of cotton 
4A 
05/31/2022 
COVID-19 & 
Specific 
(described in statistical reporting 
General 
number 6307.90.9889 prior to July 1, 
2020) 
6307.90.9891  Product 
Single-use blood pressure cuff sleeves 
4A 
05/31/2022 
COVID-19 & 
Specific 
of textile materials (described in 
General 
statistical reporting number 
6307.90.9889 prior to July 1, 2020) 
6307.90.9891  Product 
Single-use stethoscope covers 
4A 
05/31/2022 
COVID-19 & 
Specific 
(described in statistical reporting 
General 
number 6307.90.9889 prior to July 1, 
2020) 
6307.90.9891  Product 
Woven gauze sponges of cotton in 
4A 
05/31/2022 
COVID-19 & 
Specific 
square or rectangular sizes (described 
General 
in statistical reporting number 
6307.90.9889 prior to July 1, 2020) 
6505.00.8015  Entire 
Nonwoven disposable headgear 
3 
05/31/2022 
COVID-19 & 
Subheading  without peaks or visors of manmade 
General 
fibers 
8413.20.0000  Product 
Hand pumps (other than for fuel or 
3 
05/31/2022 
COVID-19 & 
Specific 
lubricants, not fitted or designed to be 
General 
fitted with a metering device), each 
used to dispense a metered quantity of 
liquid soap or sanitizer 
8413.20.0000  Product 
Hand pumps for liquids of acrylonitrile 
3 
05/31/2022 
COVID-19 & 
Specific 
butadiene styrene plastics 
General 
8421.39.8090  Product 
Disposable plastic filters of a kind 
1 
05/31/2022 
COVID-19 & 
Specific 
suitable for filtering and dehumidifying 
General 
a patient’s breath in a medical device 
such as a gas analyzer 
8424.89.9000  Product 
Dispensers of hand-cleaning or hand-
2 
05/31/2022 
COVID-19 & 
Specific 
sanitizing solutions, whether employing 
General 
a manual pump or a proximity-
detecting battery-operated pump, each 
article weighing not more than 3 kg  
8424.90.9080  Entire 
Parts of mechanical appliances for 
3 
05/31/2022 
COVID-19 & 
Subheading  projecting, dispersing, spraying 
General 
liquid/powder; spray guns and similar 
appliances, NESOI 
8531.20.0040  Product 
Indicator panels incorporating LEDs, 
3 
05/31/2022 
COVID-19 & 
Specific 
designed for use in medical infusion 
General 
equipment 
8537.10.9170  Product 
Data input devices each with display 
3 
05/31/2022 
COVID-19 
Specific 
capabilities of a kind used for magnetic 
resonance imaging equipment, 
computed tomography equipment, 
intraoperative X-ray equipment or 
patient monitors 
Congressional Research Service  
 
11 
COVID-19 and Access to Medical Products: Implications of Section 301 Tariffs 
 
Type of 
Subheading or Product 
Expiration 
HTS Code 
Exclusion 
Description 
List 
Date 
Review 
8543.10.0000  Product 
S-band and X-band linear accelerators 
1 
05/31/2022 
COVID-19 & 
Specific 
designed for use in radiation surgery 
General 
or radiation therapy equipment 
9004.90.0010  Product 
Protective articles (described in 
4A 
05/31/2022 
COVID-19 & 
Specific 
statistical reporting number 
General 
9004.90.0000 prior to January 1, 2021) 
9004.90.0090  Product 
Protective articles (described in 
4A 
05/31/2022 
COVID-19 & 
Specific 
statistical reporting number 
General 
9004.90.0000 prior to January 1, 2021) 
9011.80.0000  Product 
Compound binocular optical 
3 
05/31/2022 
COVID-19 & 
Specific 
microscopes (other than stereoscopic 
General 
microscopes and microscopes for 
photomicrography, cinemicrography or 
microprojection), each with 
magnification of 40X or more but not 
exceeding 1,000X, weighing not more 
than 3 kg 
9011.80.0000  Product 
Compound optical microscopes (other 
3 
05/31/2022 
COVID-19 & 
Specific 
than stereoscopic microscopes and 
General 
microscopes for photomicrography, 
cinemicrography or microprojection), 
each with magnification of 40X or 
more but not exceeding 400X, 
weighing not more than 15 kg 
9018.11.9000  Product 
Disposable electrocardiograph 
1 
05/31/2022 
COVID-19 & 
Specific 
electrodes 
General 
9018.12.0000  Product 
Ultrasonic scanning apparatus, each 
1 
05/31/2022 
COVID-19 
Specific 
having dimensions not exceeding 122 
cm by 77 cm by 127 cm, whether or 
not presented with transducer 
9018.19.9530  Product 
Blood pressure monitors suitable for 
1 
05/31/2022 
COVID-19 
Specific 
use by medical professionals 
9018.19.9550  Product 
Digital peak flow meters suitable for 
1 
05/31/2022 
COVID-19 & 
Specific 
use by medical professionals 
General 
9018.19.9550  Product 
Fingertip pulse oximeters suitable for 
1 
05/31/2022 
COVID-19 & 
Specific 
use by medical professionals 
General 
9018.19.9560  Product 
Disposable surface electrodes for 
1 
05/31/2022 
COVID-19 & 
Specific 
Intra-operative neuromonitoring 
General 
systems, each composed of a surface 
electrode pad, an insulated wire, and a 
standard DIN 42802 connector 
9018.19.9560  Product 
Bismuth germanate crystals with set 
1 
05/31/2022 
COVID-19 & 
Specific 
dimensional and surface finish 
General 
requirements and used as a detection 
element in Positron Emission 
Tomography detectors 
9018.19.9560  Product 
Magnetic resonance imaging patient 
1 
05/31/2022 
COVID-19 & 
Specific 
enclosure devices, each incorporating 
General 
radio frequency and gradient coils 
Congressional Research Service  
 
12 
COVID-19 and Access to Medical Products: Implications of Section 301 Tariffs 
 
Type of 
Subheading or Product 
Expiration 
HTS Code 
Exclusion 
Description 
List 
Date 
Review 
9018.19.9560  Product 
Parts and accessories of capnography 
1 
05/31/2022 
COVID-19 & 
Specific 
monitors 
General 
9018.90.2000  Product 
Otoscopes 
1 
05/31/2022 
COVID-19 & 
Specific 
General 
9018.90.3000  Product 
Anesthetic instruments and appliances 
1 
05/31/2022 
COVID-19 
Specific 
suitable for use in medical or surgical 
sciences, and parts and accessories of 
the foregoing 
9018.90.3000  Product 
Anesthesia masks 
1 
05/31/2022 
COVID-19 & 
Specific 
General 
9018.90.6000  Product 
Electrosurgical cautery pencils with 
1 
05/31/2022 
COVID-19 & 
Specific 
electrical connectors 
General 
9018.90.7580  Product 
Printed circuit board assemblies 
1 
05/31/2022 
COVID-19 & 
Specific 
designed for use in displaying 
General 
operational performance of medical 
infusion equipment 
9022.12.0000  Product 
Combined positron emission 
1 
05/31/2022 
COVID-19 & 
Specific 
tomography/computed tomography 
General 
scanners which utilize multiple PET 
gantries on a common base 
9022.90.2500  Product 
X-ray tables 
1 
05/31/2022 
COVID-19 & 
Specific 
General 
9022.90.4000  Product 
X-ray tube housings and parts thereof 
1 
05/31/2022 
COVID-19 & 
Specific 
General 
9022.90.6000  Product 
Multi-leaf col imators of radiotherapy 
1 
05/31/2022 
COVID-19 & 
Specific 
systems based on the use of X-ray 
General 
9022.90.6000  Product 
Parts and accessories, of metal, for 
1 
05/31/2022 
COVID-19 & 
Specific 
mobile X-ray apparatus 
General 
9022.90.6000  Product 
Vertical stands special y designed to 
1 
05/31/2022 
COVID-19 & 
Specific 
support, contain or adjust the 
General 
movement of X-ray digital detectors, 
or the X-ray tube and col imator in 
complete X-ray diagnostic systems 
9022.90.9500  Product 
Thermoplastic masks of 
1 
05/31/2022 
COVID-19 & 
Specific 
polycaprolactone for the use of 
General 
immobilizing patients, during the use of 
alpha, beta or gamma radiations, for 
radiography or radiotherapy 
9025.19.8010  Entire 
Clinical infrared thermometers of a 
2 
05/31/2022 
COVID-19 
Subheading  kind described in statistical note 2, not 
combined with other instruments 
9025.19.8020  Entire 
Clinical thermometers, other than 
2 
05/31/2022 
COVID-19 
Subheading  infrared, not combined with other 
instruments, NESOI 
9025.19.8060  Entire 
Infrared thermometers, other than 
2 
05/31/2022 
COVID-19 
Subheading  clinical, not combined with other 
instruments, NESOI 
Congressional Research Service  
 
13 
COVID-19 and Access to Medical Products: Implications of Section 301 Tariffs 
 
Type of 
Subheading or Product 
Expiration 
HTS Code 
Exclusion 
Description 
List 
Date 
Review 
9025.19.8085  Entire 
Thermometers, not combined with 
2 
05/31/2022 
COVID-19 
Subheading  other instruments, NESOI 
9027.90.5650  Product 
Inoculator sets of plastics, each 
1 
05/31/2022 
COVID-19 & 
Specific 
consisting of a plate with multiple 
General 
wells, a display tray, and a lid; when 
assembled, the set measuring 105 mm 
or more but not exceeding 108 mm in 
width, 138 mm or more but not 
exceeding 140 mm in depth, and 6.5 
mm or less in thickness 
Source: Congressional Research Service and the Office of the U.S. Trade Representative. 
Notes: NESOI: not elsewhere specified or included. Products covered by Lists 1 through 3 are subject to 
additional Section 301 tariffs (ad valorem) of 25%, while those under List 4A are subject to a 7.5% additional tariff. 
The time window to submit comments as part of the “COVID-19 Review” opened on August 27 and closed on 
September 27, 2021, while the comment window for the “General Review” opened on October 12 and is to 
close on December 1, 2021. The 99 exclusions expiring on November 30, 2021, are reflected in 84 special y 
prepared product descriptions and 33 10-digit Harmonized Tariff Schedule of the United States (HTS) 
subheadings. [*] In October 2020, the USTR made a technical amendment to this product specific exclusion. Its 
original description was “‘Mixtures containing 2-(dimethylamino) ethanol (CAS No. 108–01–0).” For more detail, 
see Office of the U.S. Trade Representative, “Notice of Product Exclusion Extension Amendments: China’s Acts, 
Policies, and Practices Related to Technology Transfer, Intellectual Property, and Innovation,” 85 FR 63332, 
October 7, 2020. 
Table 2. Section 301 Tariff Exclusion Extensions Under Review: Other Products With 
Potential Uses For COVID-19 Response Efforts 
Type of 
Subheading or Product 
Expiration 
HTS Code 
Exclusion 
Description 
List 
Date 
Review 
8409.91.9990  Product 
Hydraulic valve lifters of steel with 
3 
Expired 
General 
Specific 
rol ers, suitable for use solely or 
(12/31/2020) 
principally with spark-ignition internal 
combustion piston engines (other than 
for aircraft engines, marine propulsion 
engines or for vehicles of subheading 
8701.20, or headings 8702, 8703 or 
8704), each measuring 5 cm or more 
but not over 13 cm in length and 2.5 
cm or more but not over 3.9 cm in 
diameter and weighing 135 g or more 
but not over 410 g [e.g., for 
ambulances] 
8409.91.9990  Product 
Solid valve lifters of steel, suitable for 
3 
Expired 
General 
Specific 
use solely or principally with spark-
(12/31/2020) 
ignition internal combustion piston 
engines (other than for aircraft 
engines, marine propulsion engines or 
for vehicles of subheading 8701.20, or 
headings 8702, 8703 or 8704), each 
measuring 19 mm or more but not 
over 114 mm in length and 6 mm or 
more but not over 26 mm in diameter 
and weighing 20 g or more but not 
over 250 g [e.g., for ambulances] 
Congressional Research Service  
 
14 
COVID-19 and Access to Medical Products: Implications of Section 301 Tariffs 
 
Type of 
Subheading or Product 
Expiration 
HTS Code 
Exclusion 
Description 
List 
Date 
Review 
8413.30.9090  Product 
Cooling medium pumps for internal 
3 
Expired 
General 
Specific 
combustion piston engines of the 
(12/31/2020) 
motor vehicles of headings 8703 or 
8704 [e.g., for ambulances] 
8421.39.8015  Product 
Air purification equipment, electrically 
1 
Expired 
General 
Specific 
powered, weighing less than 36 kg 
(12/31/2020) 
9011.10.8000  Product 
Stereoscopic microscopes, not 
1 
Expired 
General 
Specific 
provided with a means for 
(12/31/2020) 
photographing the image, valued not 
over $500 per unit 
9011.90.0000  Product 
Adapter rings, tubes and extension 
1 
Expired 
General 
Specific 
sleeves, stands and arm assemblies, 
(12/31/2020) 
stages and gliding tables, eye guards 
and focusing racks, all the foregoing 
designed for use with compound 
optical microscopes 
9018.12.0000  Product 
Portable ultrasonic scanner consoles, 
1 
Expired 
General 
Specific 
each weighing less than 4 kg, 
(12/31/2020) 
presented with or without transducer 
9022.14.0000  Product 
Radiation therapy systems, each 
1 
Expired 
General 
Specific 
encased by steel-based structural shell 
(12/27/2020) 
with gantry cover comprising three 
pairs of plastics-based panels 
9022.90.6000  Product 
Printed circuit board assemblies, of a 
1 
Expired 
General 
Specific 
kind designed for use in X-ray 
(12/31/2020) 
apparatus 
9025.19.8010  Product 
Digital clinical thermometers 
2 
Expired 
General 
Specific 
(described in statistical reporting 
(12/31/2020) 
number 9025.19.8040 prior to July 1, 
2020) 
9025.19.8010  Product 
Digital clinical thermometers, valued 
2 
Expired 
General 
Specific 
not over $11 each (described in 
(12/31/2020) 
statistical reporting number 
9025.19.8040 prior to July 1, 2020) 
9025.19.8020  Product 
Digital clinical thermometers 
2 
Expired 
General 
Specific 
(described in statistical reporting 
(12/31/2020) 
number 9025.19.8040 prior to July 1, 
2020) 
9025.19.8020  Product 
Digital clinical thermometers, valued 
2 
Expired 
General 
Specific 
not over $11 each (described in 
(12/31/2020) 
statistical reporting number 
9025.19.8040 prior to July 1, 2020) 
9403.90.8041  Product 
Bed rails, each of which attaches to 
3 
Expired 
General 
Specific 
the side of a bed to prevent the 
(12/31/2020) 
occupant of the bed from rol ing out, 
with a nylon mesh fabric cover 
Source: Congressional Research Service and the Office of the U.S. Trade Representative. 
Notes: Products covered by Lists 1 through 3 are subject to additional Section 301 tariffs (ad valorem) of 25%. 
The time window to submit comments as part of the “General Review” opened on October 12 and is to close 
on December 1, 2021. 
Congressional Research Service  
 
15 
COVID-19 and Access to Medical Products: Implications of Section 301 Tariffs 
 
 
 
Author Information 
 
Andres B. Schwarzenberg 
   
Analyst in International Trade and Finance 
    
 
 
Disclaimer 
This document was prepared by the Congressional Research Service (CRS). CRS serves as nonpartisan 
shared staff to congressional committees and Members of Congress. It operates solely at the behest of and 
under the direction of Congress. Information in a CRS Report should not be relied upon for purposes other 
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Congressional Research Service  
R46954 · VERSION 5 · UPDATED 
16