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CO2 Sampling Nasal Cannula 0502

by Westmed, Inc.

CO2 Sampling Nasal Cannula 0502 is a Class II device made by Westmed, Inc., listed in FDA GUDID since 6 Jan 2017 (UDI-DI 00709078001635), registry data as of 22 Oct 2026.

Listed FDA GUDID listing, no authorization on record

Valid until

Not applicable

Database listing, no authorization

FDA recalls

Not checked

No FDA submission to match recalls against

Documents

None

No authorization documents

Trust

Unverified

Source GUDID, synced 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00709078001635 UDI-DI Date6 Jan 2017ListedStatusListed GUDID: in commercial distribution

Official records

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade name
CO2 Sampling Nasal Cannula
Generic name
Nasal oxygen cannula, carbon-dioxide-sampling
Model / reference
0502
Primary DI / UDI-DI
00709078001635
FDA product code
CCK
GMDN term
Nasal oxygen cannula, carbon-dioxide-sampling
Device class
Class II
Regulation number
868.1400
GUDID distribution status
In Commercial Distribution

Similar devices

Other devices filed under FDA product code CCK (Analyzer, Gas, Carbon-Dioxide, Gaseous-Phase).

Other devices from Westmed, Inc.

See all devices from Westmed, Inc. →

Properties

  • Single use
  • Prescription use
  • Lot / batch number
Other properties (12, all answered No)