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826721

by Richard Wolf GmbH

Ref 8267.21Model 10000201346

826721 (8267.21) is a Class I device made by Richard Wolf GmbH, registered in EUDAMED on 1 Sep 2026 (Basic UDI-DI B-04055207039175) and listed in FDA GUDID since 21 May 2024 (UDI-DI 04055207039175), 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-04055207039175 Basic UDI-DI 04055207039175UDI-DIDate1 Sep 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number04055207039175 UDI-DI Date21 May 2024ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI B-04055207039175 registered 1 Sep 2026 Active
  • FDA GUDID UDI-DI 04055207039175 listed 21 May 2024 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 04055207039175
  2. Registered EUDAMED B-04055207039175

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  • Withdrawn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
ENT surgical procedure kit, non-medicated, reusable
Device name
Laryngeal surgery probes
Model / Ref / Catalog
10000201346, 8267.21, 826721
Description
PROBE DULL TL 265MM angled
Primary DI / UDI-DI
04055207039175
Basic UDI-DI
B-04055207039175
FDA product code
KAK
EMDN code
L140399 Larynx surgery instruments, reusable - other
GMDN term
ENT surgical procedure kit, non-medicated, 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 — 265 Millimeter

Truth per registry

2 sources · 1 field differs

FieldEUDAMEDGUDID
Model / referenceEUDAMED
10000201346
8267.21
GUDID
826721

Related devices

Category: ENT surgical procedure kit, non-medicated, reusable

Similar devices in this category

Other devices filed under LARYNX SURGERY INSTRUMENTS, REUSABLE - OTHER.

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)