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828352

by Richard Wolf GmbH

Ref 8283.52Model 10000201532

828352 (8283.52) is a Class I device made by Richard Wolf GmbH, registered in EUDAMED on 1 Sep 2026 (Basic UDI-DI B-04055207039564) and listed in FDA GUDID since 7 Dec 2022 (UDI-DI 04055207039564), 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-04055207039564 Basic UDI-DI 04055207039564UDI-DIDate1 Sep 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number04055207039564 UDI-DI Date7 Dec 2022ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI B-04055207039564 registered 1 Sep 2026 Active
  • FDA GUDID UDI-DI 04055207039564 listed 7 Dec 2022 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 04055207039564
  2. Registered EUDAMED B-04055207039564

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  • Withdrawn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 tissue manipulation forceps, reusable
Device name
ENT grasping forceps
Model / Ref / Catalog
10000201532, 8283.52, 828352
Description
GRASPING FORCEPS - MEDIUM WL 245MM jaw straight, rippled, double opening, sheath straight, reusable
Primary DI / UDI-DI
04055207039564
Basic UDI-DI
B-04055207039564
FDA product code
KAE
EMDN code
L149099 ENT instruments, reusable - other
GMDN term
Rigid endoscopic tissue manipulation forceps, reusable
Device class
Class I
Regulation number
874.4420
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 — 245 Millimeter

Truth per registry

2 sources · 1 field differs

FieldEUDAMEDGUDID
Model / referenceEUDAMED
10000201532
8283.52
GUDID
828352

Related devices

Category: Rigid endoscopic tissue manipulation forceps, reusable

Similar devices in this category

Other devices filed under ENT INSTRUMENTS, REUSABLE - OTHER.

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)