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Oxygen Mask

FDA UDI

Class I (US FDA UDI)

by Distribution Unlimited, Llc

Identity

Trade Name
Oxygen Mask FDA UDI
Generic Name
Rebreathing oxygen face mask FDA UDI
Device Name
an oxygen mask provides a method to transfer breathing oxygen gas from a storage tank to the lungs. FDA UDI
Model / Reference
1 FDA UDI
Description
an oxygen mask provides a method to transfer breathing oxygen gas from a storage tank to the lungs. FDA UDI

Identifiers

Catalog Number
DU1050 FDA UDI
Primary DI / UDI-DI
00850014433918 FDA UDI
FDA Product Code
BYG FDA UDI
GMDN Term
Rebreathing oxygen face mask FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
868.5580 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

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

Oxygen Mask by Distribution Unlimited, 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 e8782fcf-9820-4e75-b3d4-f6a327ec841e 34 fields · synced May 31, 2026