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Welch Allyn, Inc. 901058

by Welch Allyn, Inc. 47 variants

Ref 74WTModel 901058

Welch Allyn, Inc. 901058 (74WT) is a multiple physiological parameter spot-check system (EU MDD Class IIa; FDA Class II; FDA product code MWI, Monitor, physiological, patient (without arrhythmia detection or alarms)) made by Welch Allyn, Inc., registered in EUDAMED on 20 Oct 2026 (Basic UDI-DI B-00732094338768) and listed in FDA GUDID since 26 Aug 2020 (UDI-DI 00732094338768), active as of 24 Oct 2026.

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

CE MDD

Valid until

No date given

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

Source EUDAMED, GUDID, synced 24 Oct 2026.

Regulatory status

as of registry sync 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD EUDAMED NumberB-00732094338768 Basic UDI-DI 00732094338768UDI-DIDate20 Oct 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number00732094338768 UDI-DI Date26 Aug 2020ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI B-00732094338768 registered 20 Oct 2026 Active
  • FDA GUDID UDI-DI 00732094338768 listed 26 Aug 2020 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 00732094338768
  2. Registered EUDAMED B-00732094338768

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  • Withdrawn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
Welch Allyn Connex Spot Monitor EUDAMED
Welch Allyn, Inc. GUDID
Generic name
Multiple physiological parameter spot-check system, clinical
Device name
Vital Signs Monitor Core
Model / Ref / Catalog
901058, 74WT
Description
WFR CSM NIBP WA SureTemp
Primary DI / UDI-DI
00732094338768
Basic UDI-DI
B-00732094338768
FDA product code
MWI
EMDN code
Z1203020202 Transportable/portable multi–parameter patient monitors
GMDN term
Multiple physiological parameter spot-check system, clinical
Device class
Class IIa EUDAMED
Class II GUDID
Regulation number
870.2300
EU registration type
Legacy device (under a directive)
EU market of registration
Netherlands
GUDID distribution status
In Commercial Distribution

Truth per registry

2 sources · 1 field differs

FieldEUDAMEDGUDID
Device classEUDAMED
Class IIa
GUDID
Class II

Device class is stated on each registry's own scale: Class IIa in the EU (EUDAMED), Class II in the US (FDA GUDID). EU and US classes are different schemes, so this is not a disagreement.

Related devices

Category: Hearing aid enhanced audio device, teaching-environment

Similar devices in this category

Other devices filed under TRANSPORTABLE/PORTABLE MULTI–PARAMETER PATIENT MONITORS.

Other devices from Welch Allyn, Inc.

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Properties

  • Measuring function
  • Prescription use
  • Lot / batch number
Other properties (22, all answered No)