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828022

by Richard Wolf GmbH

Ref 8280.22Model 10000201066

828022 (8280.22) is a Class I device made by Richard Wolf GmbH, registered in EUDAMED on 1 Sep 2026 (Basic UDI-DI B-04055207039250) and listed in FDA GUDID since 9 Aug 2022 (UDI-DI 04055207039250), 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-04055207039250 Basic UDI-DI 04055207039250UDI-DIDate1 Sep 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number04055207039250 UDI-DI Date9 Aug 2022ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI B-04055207039250 registered 1 Sep 2026 Active
  • FDA GUDID UDI-DI 04055207039250 listed 9 Aug 2022 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 04055207039250
  2. Registered EUDAMED B-04055207039250

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  • Withdrawn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 endoscopic biopsy forceps, reusable
Model / Ref / Catalog
10000201066, 8280.22, 828022
Description
BIOPSY FORCEPS WL 270MM jaw straight, toothed, double opening, sheath straight, reusable
Primary DI / UDI-DI
04055207039250
Basic UDI-DI
B-04055207039250
FDA product code
FCL, GEN
EMDN code
L080899 Bronchoscopic surgery instruments, reusable - other
GMDN term
Rigid endoscopic biopsy forceps, reusable
Device class
Class I
Regulation number
876.1075, 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
Size
Length — 270 Millimeter

Truth per registry

2 sources · 1 field differs

FieldEUDAMEDGUDID
Model / referenceEUDAMED
10000201066
8280.22
GUDID
828022

Related devices

Category: Rigid endoscopic biopsy forceps, reusable

Similar devices in this category

Other devices filed under THORACIC SURGERY INSTRUMENTS, REUSABLE.

Other devices from Richard Wolf GmbH

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Properties

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