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NA CO2 / O2 Nasal Cannula - Infant/Neonate

by Philips Medizin Systeme Böblingen GmbH

Listed FDA GUDID listing, not in commercial distribution

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

Registry data, not yet checked by deviCERTS. Source GUDID, synced 23 Oct 2026. What this means

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number20884838071982 UDI-DI Date10 Nov 2016ListedStatusListed GUDID: not in commercial distribution

Coverage

1 jurisdiction

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  • Withdrawn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

United States — GUDID listing Listed

Specification

GUDID

Generic Name
Nasal oxygen cannula, carbon-dioxide-sampling
Model / Ref / Catalog
CO2 / O2 Nasal Cannula - Infant/Neonate, 989803144471
Primary DI / UDI-DI
20884838071982
FDA Product Code
CCK
GMDN Term
Nasal oxygen cannula, carbon-dioxide-sampling
Device Class
Class II
Regulation Number
868.1400
GUDID distribution status
Not in Commercial Distribution

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Properties

  • Single Use
  • Prescription Use
  • Lot / Batch Number

Other properties (11)

  • Sterile: No
  • Implantable: No
  • Contains Latex: No
  • Over-the-Counter: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Premarket Exempt: No
  • Serial Number: No
  • Expiration Date: No
  • Manufacturing Date: No