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Welch Allyn, Inc. 901060

by Welch Allyn, Inc. 51 variants

Ref 68NXTX-BModel 901060

Welch Allyn, Inc. 901060 (68NXTX-B) is a device classified as Class IIb in the EU and Class II in the US made by Welch Allyn, Inc., registered in EUDAMED on 3 Aug 2026 (Basic UDI-DI B-00732094150810) and listed in FDA GUDID since 5 Dec 2017 (UDI-DI 00732094150810), 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-00732094150810 Basic UDI-DI 00732094150810UDI-DIDate3 Aug 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number00732094150810 UDI-DI Date5 Dec 2017ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI B-00732094150810 registered 3 Aug 2026 Active
  • FDA GUDID UDI-DI 00732094150810 listed 5 Dec 2017 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 00732094150810
  2. Registered EUDAMED B-00732094150810

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  • Withdrawn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 Vital Signs Monitor EUDAMED
Welch Allyn, Inc. GUDID
Generic name
General-purpose multi-parameter bedside monitor
Model / Ref / Catalog
901060, 68NXTX-B
Primary DI / UDI-DI
00732094150810
Basic UDI-DI
B-00732094150810
FDA product code
MWI
EMDN code
Z1203020201 Multi–parameter patient bedside monitors
GMDN term
General-purpose multi-parameter bedside monitor
Device class
Class IIb 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 IIb
GUDID
Class II

Device class is stated on each registry's own scale: Class IIb 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: General-purpose multi-parameter bedside monitor

Similar devices in this category

Other devices filed under MULTI–PARAMETER PATIENT BEDSIDE MONITORS.

Other devices from Welch Allyn, Inc.

See all devices from Welch Allyn, Inc. →

Properties

  • Measuring function
  • Prescription use
  • Serial number
  • Manufacturing date
Other properties (21, all answered No)