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891737080

by Richard Wolf GmbH

Ref 891737080Model 10000201191

891737080 is a device classified as Class IIa in the EU and Class I in the US made by Richard Wolf GmbH, registered in EUDAMED on 1 Sep 2026 (Basic UDI-DI B-04055207034910) and listed in FDA GUDID since 3 Aug 2022 (UDI-DI 04055207034910), 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-04055207034910 Basic UDI-DI 04055207034910UDI-DIDate1 Sep 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number04055207034910 UDI-DI Date3 Aug 2022ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI B-04055207034910 registered 1 Sep 2026 Active
  • FDA GUDID UDI-DI 04055207034910 listed 3 Aug 2022 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 04055207034910
  2. Registered EUDAMED B-04055207034910

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  • Withdrawn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
General-purpose endoscopic needle, reusable
Device name
Rigid arthroscopic irrigation cannula
Model / Ref / Catalog
891737080, 10000201191
Description
CANNULA FOR IRRIGATION Ø 8MM WL 168MM reusable
Primary DI / UDI-DI
04055207034910
Basic UDI-DI
B-04055207034910
FDA product code
NBH
EMDN code
L1907 Arthroscopic surgery cannulas, reusable
GMDN term
General-purpose endoscopic needle, reusable
Device class
Class IIa EUDAMED
Class I GUDID
Regulation number
888.1100
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
Length — 168 Millimeter
Outer Diameter — 8 Millimeter

Truth per registry

2 sources · 1 field differs

FieldEUDAMEDGUDID
Device classEUDAMED
Class IIa
GUDID
Class I

Device class is stated on each registry's own scale: Class IIa in the EU (EUDAMED), Class I in the US (FDA GUDID). EU and US classes are different schemes, so this is not a disagreement.

Related devices

Category: General-purpose endoscopic needle, reusable

Similar devices in this category

Other devices filed under ARTHROSCOPIC SURGERY CANNULAS, REUSABLE.

Other devices from Richard Wolf GmbH

See all devices from Richard Wolf GmbH →

Properties

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