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Cable PTO 095624-001

by Raumedic AG

Ref 095624-001

Cable PTO 095624-001 is a device classified as Class I in the EU and Class II in the US made by Raumedic AG, registered in EUDAMED on 10 Jun 2026 (Basic UDI-DI 4057834ZubKaPTO00366K) and listed in FDA GUDID since 18 Aug 2016 (UDI-DI 04057834030099), active as of 12 Nov 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 12 Nov 2026.

Regulatory status

as of registry sync 12 Nov 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR EUDAMED Number4057834ZubKaPTO00366K Basic UDI-DI 04057834030099UDI-DIDate10 Jun 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number04057834030099 UDI-DI Date18 Aug 2016ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI 4057834ZubKaPTO00366K registered 10 Jun 2026 Active
  • FDA GUDID UDI-DI 04057834030099 listed 18 Aug 2016 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 04057834030099
  2. Registered EUDAMED 4057834ZubKaPTO00366K

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  • Withdrawn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
Cable PTO
Generic name
Electrical-only medical device connection cable, reusable
Model / reference
095624-001
Primary DI / UDI-DI
04057834030099
Basic UDI-DI
4057834ZubKaPTO00366K
FDA product code
GWM
EMDN code
V9099 Various devices not included in other classes - other
GMDN term
Electrical-only medical device connection cable, reusable
Device class
Class I EUDAMED
Class II GUDID
Regulation number
882.1620
EU registration type
Standard device
EU market of registration
Germany
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: Electrical-only medical device connection cable, reusable

Similar devices in this category

Other devices filed under VARIOUS DEVICES NOT INCLUDED IN OTHER CLASSES - OTHER.

Other devices from Raumedic AG

See all devices from Raumedic AG →

Properties

  • Prescription use
  • Serial number
  • Manufacturing date
Other properties (22, all answered No)