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8965141

by Richard Wolf GmbH

Ref 8965.141Model 10000201307

8965141 (8965.141) is a device classified as Class I in the EU and Class II in the US made by Richard Wolf GmbH, registered in EUDAMED on 1 Sep 2026 (Basic UDI-DI B-04055207023303) and listed in FDA GUDID since 3 Mar 2021 (UDI-DI 04055207023303), active as of 23 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 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD EUDAMED NumberB-04055207023303 Basic UDI-DI 04055207023303UDI-DIDate1 Sep 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number04055207023303 UDI-DI Date3 Mar 2021ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI B-04055207023303 registered 1 Sep 2026 Active
  • FDA GUDID UDI-DI 04055207023303 listed 3 Mar 2021 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 04055207023303
  2. Registered EUDAMED B-04055207023303

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  • Withdrawn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

Generic name
Rigid endoscope obturator
Device name
Obturators
Model / Ref / Catalog
10000201307, 8965.141, 8965141
Description
OBTURATOR FOR NEPHROSCOPE 24FR WL 229mm, round, cannulated, rounded distal end, compatible with sheath 8965041, reusable
Primary DI / UDI-DI
04055207023303
Basic UDI-DI
B-04055207023303
FDA product code
FEC
EMDN code
L060408 Endoscopic urology fillers, reusable
GMDN term
Rigid endoscope obturator
Device class
Class I EUDAMED
Class II GUDID
Regulation number
876.1500
EU registration type
Legacy device (under a directive)
EU market of registration
Germany
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization
Size
Outer Diameter — 8 Millimeter

Truth per registry

2 sources · 2 fields differ

FieldEUDAMEDGUDID
Model / referenceEUDAMED
10000201307
8965.141
GUDID
8965141
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: Rigid endoscope obturator

Similar devices in this category

Other devices filed under ENDOSCOPIC UROLOGY INSTRUMENTS, REUSABLE.

Other devices from Richard Wolf GmbH

See all devices from Richard Wolf GmbH →

Properties

  • Sterilise before use
  • Reusable
  • Lot / batch number
  • Manufacturing date
Other properties (21, all answered No)