Skip to content

826710

by Richard Wolf GmbH

Ref 8267.10Model 10000201343

826710 (8267.10) is a Class I device made by Richard Wolf GmbH, registered in EUDAMED on 5 Oct 2026 (Basic UDI-DI B-04055207039137) and listed in FDA GUDID since 9 Aug 2022 (UDI-DI 04055207039137), 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-04055207039137 Basic UDI-DI 04055207039137UDI-DIDate5 Oct 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number04055207039137 UDI-DI Date9 Aug 2022ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI B-04055207039137 registered 5 Oct 2026 Active
  • FDA GUDID UDI-DI 04055207039137 listed 9 Aug 2022 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 04055207039137
  2. Registered EUDAMED B-04055207039137

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  • Withdrawn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
Tonsil knife
Device name
Laryngoscopic knives
Model / Ref / Catalog
10000201343, 8267.10, 826710
Description
SICKLE KNIFE TL 262MM curved, reusable
Primary DI / UDI-DI
04055207039137
Basic UDI-DI
B-04055207039137
FDA product code
JZY
EMDN code
L140301 Larynx surgery scalpels, reusable
GMDN term
Tonsil knife
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 — 262 Millimeter

Truth per registry

2 sources · 1 field differs

FieldEUDAMEDGUDID
Model / referenceEUDAMED
10000201343
8267.10
GUDID
826710

Related devices

Category: Tonsil knife

Similar devices in this category

Other devices filed under LARYNX SURGERY INSTRUMENTS, REUSABLE.

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)