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989803159631

by Philips Medizin Systeme Böblingen GmbH

989803159631 is a Class II device made by Philips Medizin Systeme Böblingen GmbH, listed in FDA GUDID since 22 Nov 2016 (UDI-DI 00884838073593), registry data as of 23 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 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00884838073593 UDI-DI Date22 Nov 2016ListedStatusListed 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  • Withdrawn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

Generic name
Transcutaneous blood gas monitor sensor
Model / Ref / Catalog
989803159631
Primary DI / UDI-DI
00884838073593
FDA product code
MHX
GMDN term
Transcutaneous blood gas monitor sensor
Device class
Class II
Regulation number
870.1025
GUDID distribution status
In Commercial Distribution

Related devices

Category: Transcutaneous blood gas monitor sensor

Similar devices in this category

Other devices filed under Transcutaneous blood gas monitor sensor.

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Properties

  • Serial number
Other properties (14, all answered No)