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MedSource Face Mask

FDA UDI

Class N (US FDA UDI)

by Medsource International Llc

Identity

Trade Name
MedSource Face Mask FDA UDI
Generic Name
Aerosol face mask, rebreathing, single-use FDA UDI
Device Name
Face Mask, Padded, Neonatal, Ambu FDA UDI
Model / Reference
MS-21131 FDA UDI
Description
Face Mask, Padded, Neonatal, Ambu FDA UDI

Identifiers

Catalog Number
Not Applicable FDA UDI
Primary DI / UDI-DI
00816703025864 FDA UDI
FDA Product Code
QKR FDA UDI
GMDN Term
Aerosol face mask, rebreathing, single-use FDA UDI

Classification

Device Class
N 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

Yes

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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Aerosol face mask, rebreathing, single-use

MedSource Face Mask by Medsource International Llc — Class N — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Aerosol face mask, rebreathing, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 69532fb6-2d83-4fed-8045-90c281f27f51 34 fields · synced May 30, 2026