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NA Reusable Infant Airway Adapter

by Philips Medizin Systeme Böblingen GmbH GUDID

Listed FDA GUDID listing, not in commercial distribution

Regulatory status

as of 29 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00884838072169 UDI-DIDate4 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  • Withdrawn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

Recalls

0 recalls · FDA

No FDA recalls on record, checked 23 Oct 2026.

Specification

GUDID

Generic Name
Carbon dioxide cuvette, reusable
Model / Ref / Catalog
Reusable Infant Airway Adapter, 989803142691
Primary DI / UDI-DI
00884838072169
FDA Product Code
MHX
GMDN Term
Carbon dioxide cuvette, reusable
Device Class
Class II
Regulation Number
870.1025
GUDID distribution status
Not in Commercial Distribution

Other devices from Philips Medizin Systeme Böblingen GmbH

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Properties

  • Prescription Use
  • Lot / Batch Number

Other properties (12)

  • Sterile: No
  • Single Use: 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