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McKesson

FDA UDI

Class II (US FDA UDI)

by Mckesson Medical-Surgical Inc.

Identity

Trade Name
McKesson FDA UDI
Generic Name
Surgical/medical respirator, non-antimicrobial, single-use FDA UDI
Device Name
Ultra Sensitive FogFree Procedural Ear Loop Mask w/ Secure Fit Technology and Shield, white (ASTM Level 3 w/ shield) FDA UDI
Model / Reference
73-GCPWSSF FDA UDI
Description
Ultra Sensitive FogFree Procedural Ear Loop Mask w/ Secure Fit Technology and Shield, white (ASTM Level 3 w/ shield) FDA UDI

Identifiers

Primary DI / UDI-DI
20612479229406 FDA UDI
FDA Product Code
FXX FDA UDI
GMDN Term
Surgical/medical respirator, non-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

No

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

Yes

FDA UDI

Category: Surgical/medical respirator, non-antimicrobial, single-use

McKesson by Mckesson Medical-Surgical Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Surgical/medical respirator, non-antimicrobial, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Mckesson Medical-Surgical Inc.

Sources (1)

  • FDA UDI cfc41503-8dc1-4d9c-8be9-7d00182236c3 33 fields · synced May 30, 2026