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Welch Allyn, Inc. 901041

by Welch Allyn, Inc. 9 variants

Ref DS48AModel 901041

Welch Allyn, Inc. 901041 (DS48A) is a device classified as Class I in the EU and Class II in the US made by Welch Allyn, Inc., registered in EUDAMED on 29 Oct 2026 (Basic UDI-DI B-00732094083866) and listed in FDA GUDID since 17 Sep 2016 (UDI-DI 00732094083866), active as of 7 Nov 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 7 Nov 2026.

Regulatory status

as of registry sync 7 Nov 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD EUDAMED NumberB-00732094083866 Basic UDI-DI 00732094083866UDI-DIDate29 Oct 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number00732094083866 UDI-DI Date17 Sep 2016ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI B-00732094083866 registered 29 Oct 2026 Active
  • FDA GUDID UDI-DI 00732094083866 listed 17 Sep 2016 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 00732094083866
  2. Registered EUDAMED B-00732094083866

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  • Withdrawn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 Durashock Gauges EUDAMED
Welch Allyn, Inc. GUDID
Generic name
Blood pressure cuff, reusable
Device name
Gauge, Hand Held
Model / Ref / Catalog
901041, DS48A
Primary DI / UDI-DI
00732094083866
Basic UDI-DI
B-00732094083866
FDA product code
DXQ
EMDN code
C9006 Aneroid sphygmomanometers
GMDN term
Blood pressure cuff, reusable
Device class
Class I EUDAMED
Class II GUDID
Regulation number
870.1120
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 I
GUDID
Class II

Device class is stated on each registry's own scale: Class I 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: Blood pressure cuff, reusable

Similar devices in this category

Other devices filed under ANEROID SPHYGMOMANOMETERS.

Other devices from Welch Allyn, Inc.

See all devices from Welch Allyn, Inc. →

Properties

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