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Riwomobil 32116013

by Richard Wolf GmbH

Ref 32116013Model 10000201479

Riwomobil 32116013 is a Class I device made by Richard Wolf GmbH, registered in EUDAMED on 22 Jul 2026 (Basic UDI-DI 405520711062019-0028611EJ) and listed in FDA GUDID since 6 Aug 2024 (UDI-DI 04055207025024), active as of 23 Oct 2026.

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

CE MDR

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 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR EUDAMED Number405520711062019-0028611EJ Basic UDI-DI 04055207025024UDI-DIDate22 Jul 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number04055207025024 UDI-DI Date6 Aug 2024ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI 405520711062019-0028611EJ registered 22 Jul 2026 Active
  • FDA GUDID UDI-DI 04055207025024 listed 6 Aug 2024 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 04055207025024
  2. Registered EUDAMED 405520711062019-0028611EJ

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  • Withdrawn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
Riwomobil
Generic name
Medical device integration rack
Device name
Mobile device carts and support arms
Model / Ref / Catalog
32116013, 10000201479
Primary DI / UDI-DI
04055207025024
Basic UDI-DI
405520711062019-0028611EJ
Direct marketing DI
04055207025024
FDA product code
FEM
EMDN code
Z12029003 Endoscope transport carts
GMDN term
Medical device integration rack
Device class
Class I
Regulation number
876.1500
EU registration type
Standard device
EU market of registration
Germany
GUDID distribution status
In Commercial Distribution

Related devices

Category: Medical device integration rack

Similar devices in this category

Other devices filed under ENDOSCOPE TRANSPORT CARTS.

Other devices from Richard Wolf GmbH

See all devices from Richard Wolf GmbH →

Properties

  • Premarket exempt
  • Serial number
  • Manufacturing date
Other properties (22, all answered No)