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Jemsdal

FDA UDI

Class I (US FDA UDI)

by Canadian Hospital Specialties Limited

Identity

Trade Name
Jemsdal FDA UDI
Generic Name
Rebreathing oxygen face mask FDA UDI
Device Name
MASK SMALL ADULT JEMSDAL W/ 7' SAFLO OXYGEN TUBING ETCO2 CONNECTOR FDA UDI
Model / Reference
A-251 FDA UDI
Description
MASK SMALL ADULT JEMSDAL W/ 7' SAFLO OXYGEN TUBING ETCO2 CONNECTOR FDA UDI

Identifiers

Catalog Number
A-251 FDA UDI
Primary DI / UDI-DI
00628725097022 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

Jemsdal 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 8f479431-58c7-40e8-937a-a1d7dfa675f0 35 fields · synced May 30, 2026