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Philips Water Trap

by Philips Medizin Systeme Böblingen GmbH

Ref 989803191081Model Philips Watertrap

Active European Union. Also listed in GUDID (US), partly in commercial distribution.

CE MDD

Valid until

Not listed

EUDAMED holds no validity date

FDA recalls

Not checked

No FDA submission to match recalls against

Documents

None linked in EUDAMED

A group certificate may exist

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source EUDAMED, GUDID, synced 24 Oct 2026. What this means

Regulatory status

as of registry sync 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD EUDAMED NumberB-00884838072251 Basic UDI-DI Date20 May 2025RegisteredStatusActive
United StatesGUDID listing GUDID Number00884838072251 UDI-DI Date29 Nov 2016ListedStatusListed GUDID: 1 of 2 UDI-DIs in commercial distribution

Certificates

0 certificates · EUDAMED

EUDAMED lists no certificate for this device's Basic UDI-DI.

A certificate issued for a device group may exist without being linked here.

Coverage

2 jurisdictions

United States of AmericaSwedenFinlandLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaAustriaHungaryRomaniaSloveniaBulgariaPortugalSpainItalyCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered
  • European Union CE/MDD Active
  • United States GUDID listing Listed

Specification

EUDAMED · GUDID

Trade Name
Philips Water Trap EUDAMED
Water Trap GUDID
Generic Name
Breathing circuit condensate trap, reusable
Device Name
Philips Watertrap
Model / Ref / Catalog
989803191081, Philips Watertrap, Philips Water Trap
Primary DI / UDI-DI
00884838072251, 00884838124073
Basic UDI-DI
B-00884838072251, 0884838BM625T8
Unit of Use DI
10884838124070
FDA Product Code
CBS
EMDN Code
Z1203020299 Multi–parameter monitors - other
GMDN Term
Breathing circuit condensate trap, reusable
Device Class
Class IIb EUDAMED
Class IIa EUDAMED
Class II GUDID
Regulation Number
868.1620
EU market of registration
Austria
GUDID distribution status
Not in Commercial Distribution (UDI-DI 00884838072251)
In Commercial Distribution (UDI-DI 00884838124073)

Truth per registry

2 sources · 2 fields differ

FieldEUDAMEDGUDID
Model / ReferenceEUDAMED
989803191081
Philips Watertrap
GUDID
Philips Water Trap
Device ClassEUDAMED
Class IIb
Class IIa
GUDID
Class II

Manufacturer details

EUDAMED SRN
DE-MF-000006026

Other devices from Philips Medizin Systeme Böblingen GmbH

See all devices from Philips Medizin Systeme Böblingen GmbH →

Properties

  • Prescription Use
  • Lot / Batch Number
  • Expiration Date YesGUDIDNoGUDID
  • Manufacturing Date YesGUDIDNoGUDID

Other properties (20)

  • Sterile: No
  • Single Use: No
  • Implantable: No
  • Reusable: No
  • Contains Latex: No
  • Reprocessed: No
  • CMR Substance: No
  • Human-derived: No
  • Human Tissues: No
  • Animal Tissues: No
  • Endocrine Disruptor: No
  • Administering Medicine: No
  • Measuring Function: No
  • Incorporates Medicinal Product: No
  • Over-the-Counter: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Premarket Exempt: No
  • Serial Number: No