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MedSource Mask

FDA UDI

Class I (US FDA UDI)

by Medsource International Llc

Identity

Trade Name
MedSource Mask FDA UDI
Generic Name
Rebreathing oxygen face mask FDA UDI
Device Name
Mask, Pocket, No Case FDA UDI
Model / Reference
MS-PM100 FDA UDI
Description
Mask, Pocket, No Case FDA UDI

Identifiers

Catalog Number
Not Applicable FDA UDI
Primary DI / UDI-DI
00816703027721 FDA UDI
FDA Product Code
KGB FDA UDI
GMDN Term
Rebreathing oxygen face mask FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
868.5570 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: Rebreathing oxygen face mask

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

Similar devices

Also classified as Rebreathing oxygen face mask.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 42426117-c060-4276-be97-a675b4a57adb 34 fields · synced May 30, 2026