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828244

by Richard Wolf GmbH

Ref 828.244Model 10000201284

828244 (828.244) 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-04055207009581) and listed in FDA GUDID since 28 Sep 2016 (UDI-DI 04055207009581), 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-04055207009581 Basic UDI-DI 04055207009581UDI-DIDate1 Sep 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number04055207009581 UDI-DI Date28 Sep 2016ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI B-04055207009581 registered 1 Sep 2026 Active
  • FDA GUDID UDI-DI 04055207009581 listed 28 Sep 2016 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 04055207009581
  2. Registered EUDAMED B-04055207009581

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  • Withdrawn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
Flexible endoscopic scissors, reusable
Device name
Flex. grasping/biopsy forceps, scissors
Model / Ref / Catalog
10000201284, 828.244, 828244
Description
FLEX. SCISSORS 4FR WL 230MM toothing, double action, TL 350 mm, non-dismantling, reusable
Primary DI / UDI-DI
04055207009581
Basic UDI-DI
B-04055207009581
FDA product code
FAJ
EMDN code
L060403 Endoscopic urology forceps, reusable
GMDN term
Flexible endoscopic scissors, reusable
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
Length — 230 Millimeter
Outer Diameter — 1.33333333333 Millimeter

Truth per registry

2 sources · 2 fields differ

FieldEUDAMEDGUDID
Model / referenceEUDAMED
10000201284
828.244
GUDID
828244
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: Flexible endoscopic scissors, reusable

Similar devices in this category

Other devices filed under ENDOSCOPIC UROLOGY FORCEPS, 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)