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Cdc

FDA UDI

Class II (US FDA UDI)

by Apothecary Products, Inc.

Identity

Trade Name
CDC FDA UDI
Generic Name
Surgical/medical face mask, antimicrobial, single-use FDA UDI
Device Name
620 EARLOOP MASK FDA UDI
Model / Reference
F405-620CD FDA UDI
Description
620 EARLOOP MASK FDA UDI

Identifiers

Primary DI / UDI-DI
00840986020131 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
Not 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

Cdc by Apothecary Products, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI dc5f9529-2f8d-49d1-a330-79c2a6e6832a 35 fields · synced Jun 7, 2026