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Vital Signs™ Reusable Temperature probes, 400-Series, General Purpose probe, adult, 3 m/10 ft

by AirLife Finland Oy

Ref M1024247

Withdrawn Withdrawn in European Union. No longer placed on the EU market.

Was authorized under CE MDD, withdrawn

Ended

Withdrawn

Date not published (CE MDD)

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 25 Oct 2026. What this means

Regulatory status

as of registry sync 25 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD EUDAMED NumberB-10190752188051 Basic UDI-DI 10190752188051UDI-DIDate25 Nov 2021RegisteredStatusWithdrawn No longer placed on the EU market
United StatesGUDID listing GUDID Number10190752188051 UDI-DI Date1 Feb 2021ListedStatusListed 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  • Withdrawn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  • European Union CE/MDD Withdrawn
  • United States GUDID listing Listed

Specification

EUDAMED · GUDID

Trade Name
Vital Signs™ Reusable Temperature probes, 400-Series, General Purpose probe, adult, 3 m/10 ft EUDAMED
Vital Signs™ GUDID
Generic Name
General-purpose patient temperature probe, reusable
Device Name
Vital Signs™ Reusable Temperature probes
Model / Ref / Catalog
M1024247
Primary DI / UDI-DI
10190752188051
Basic UDI-DI
B-10190752188051
FDA Product Code
FLL
EMDN Code
V03010299 Body temperature monitoring probes - other
GMDN Term
General-purpose patient temperature probe, reusable
Device Class
Class IIa EUDAMED
Class II GUDID
Regulation Number
880.2910
EU market of registration
Finland
GUDID distribution status
In Commercial Distribution
MRI Safety
MR Unsafe

Truth per registry

2 sources · 1 field differs

FieldEUDAMEDGUDID
Device ClassEUDAMED
Class IIa
GUDID
Class II

Manufacturer details

EUDAMED SRN
FI-MF-000001482

Other devices from AirLife Finland Oy

See all devices from AirLife Finland Oy →

Properties

  • Prescription Use
  • Lot / Batch Number
  • Manufacturing Date

Other properties (19)

  • Sterile: No
  • Single Use: No
  • Implantable: No
  • Reusable: No
  • Contains Latex: No
  • Reprocessed: No
  • Human-derived: No
  • Human Tissues: No
  • Animal Tissues: 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
  • Expiration Date: No