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8934915

by Richard Wolf GmbH

Ref 8934.915Model 10000201327

8934915 (8934.915) is a Class I device made by Richard Wolf GmbH, registered in EUDAMED on 3 Sep 2026 (Basic UDI-DI B-04055207022832) and listed in FDA GUDID since 21 May 2024 (UDI-DI 04055207022832), 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-04055207022832 Basic UDI-DI 04055207022832UDI-DIDate3 Sep 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number04055207022832 UDI-DI Date21 May 2024ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI B-04055207022832 registered 3 Sep 2026 Active
  • FDA GUDID UDI-DI 04055207022832 listed 21 May 2024 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 04055207022832
  2. Registered EUDAMED B-04055207022832

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  • Withdrawn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
Laparoscopic access cannula, reusable
Device name
Surgical laparoscopic sealing cones
Model / Ref / Catalog
10000201327, 8934.915, 8934915
Description
SEALING CONE Ø 10-12MM for subcutaneous fascia suture, reusable
Primary DI / UDI-DI
04055207022832
Basic UDI-DI
B-04055207022832
FDA product code
HCF
EMDN code
L1299 Laparoscopic and thoracoscopic instruments, reusable - other
GMDN term
Laparoscopic access cannula, reusable
Device class
Class I
Regulation number
878.4800
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

Truth per registry

2 sources · 1 field differs

FieldEUDAMEDGUDID
Model / referenceEUDAMED
10000201327
8934.915
GUDID
8934915

Related devices

Category: Laparoscopic access cannula, reusable

Similar devices in this category

Other devices filed under LAPAROSCOPIC AND THORACOSCOPIC SURGERY INSTRUMENTS, REUSABLE.

Other devices from Richard Wolf GmbH

See all devices from Richard Wolf GmbH →

Properties

  • Sterilise before use
  • Reusable
  • Premarket exempt
  • Lot / batch number
  • Manufacturing date
Other properties (20, all answered No)