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Temperature Sensor (Esophageal/Rectal/Ax

by Philips Medizin Systeme Böblingen GmbH

Ref 989803194511Model Reusable Temp Probe and Disp Jacket

Active European Union. Also listed in GUDID (US).

CE MDR

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 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR EUDAMED Number0884838BM1078ME Basic UDI-DI 00884838111479UDI-DIDate2 Jun 2025RegisteredStatusActive
United StatesGUDID listing GUDID Number00884838111479 UDI-DI Date30 May 2025ListedStatusListed GUDID: 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  • Withdrawn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/MDR Active
  • United States GUDID listing Listed

Specification

EUDAMED · GUDID

Trade Name
Temperature Sensor (Esophageal/Rectal/Ax EUDAMED
MR Patient Care Temperature Sensor (Esophageal / Rectal / Axillary, Direct Mode) GUDID
Generic Name
General-purpose patient temperature probe, reusable
Device Name
Reusable Temp Probe and Disp Jacket
Model / Ref / Catalog
Reusable Temp Probe and Disp Jacket, 989803194511, Temperature Sensor (Esophageal/Rectal/Ax
Primary DI / UDI-DI
00884838111479
Basic UDI-DI
0884838BM1078ME
Direct Marketing DI
00884838111479
FDA Product Code
MWI
EMDN Code
Z1203020299 Multi–parameter monitors - other
GMDN Term
General-purpose patient temperature probe, reusable
Device Class
Class IIa EUDAMED
Class II GUDID
Regulation Number
870.2300
EU market of registration
Austria
GUDID distribution status
In Commercial Distribution
MRI Safety
MR Safe

Truth per registry

2 sources · 2 fields differ

FieldEUDAMEDGUDID
Model / ReferenceEUDAMED
Reusable Temp Probe and Disp Jacket
989803194511
GUDID
Temperature Sensor (Esophageal/Rectal/Ax
Device ClassEUDAMED
Class IIa
GUDID
Class II

Manufacturer details

EUDAMED SRN
DE-MF-000006026

Other devices from Philips Medizin Systeme Böblingen GmbH

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Properties

  • Prescription Use
  • Serial Number

Other properties (22)

  • 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
  • Lot / Batch Number: No
  • Expiration Date: No
  • Manufacturing Date: No