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Adult Oxygen Mask

FDA UDI

Class I (US FDA UDI)

by Canadian Hospital Specialties Limited

Identity

Trade Name
Adult Oxygen Mask FDA UDI
Generic Name
Rebreathing oxygen face mask FDA UDI
Device Name
Face mask, Adult, High Concentration, 7ft. Saflo Tube - multi-fit on one end FDA UDI
Model / Reference
R-2250SM FDA UDI
Description
Face mask, Adult, High Concentration, 7ft. Saflo Tube - multi-fit on one end FDA UDI

Identifiers

Primary DI / UDI-DI
00628725096919 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

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

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Rebreathing oxygen face mask

Adult Oxygen Mask by Canadian Hospital Specialties Limited — 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 2dd497ac-4b06-4217-a949-313329c11131 34 fields · synced May 30, 2026