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Cardinal Health

FDA UDI

Class II (US FDA UDI)

by Cardinal Health 200, LLC

Identity

Trade Name
CARDINAL HEALTH FDA UDI
Generic Name
Surgical/medical face mask, antimicrobial, single-use FDA UDI
Device Name
Level 3 Surgical Mask Dye-Free with anti-fog FDA UDI
Model / Reference
AT73635 FDA UDI
Description
Level 3 Surgical Mask Dye-Free with anti-fog FDA UDI

Identifiers

Catalog Number
AT73635 FDA UDI
Primary DI / UDI-DI
20885380169806 FDA UDI
FDA Product Code
FXX FDA UDI
GMDN Term
Surgical/medical face mask, antimicrobial, single-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
878.4040 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

FDA UDI

Over-the-Counter

Yes

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Surgical/medical face mask, antimicrobial, single-use

Cardinal Health by Cardinal Health 200, LLC — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Surgical/medical face mask, antimicrobial, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Cardinal Health 200, LLC

Sources (1)

  • FDA UDI 98f09b0c-d715-4ccc-8d8c-971645ce119c 34 fields · synced Jun 8, 2026