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722360

by Richard Wolf GmbH

Ref 7223.60Model 10000201282

722360 (7223.60) is a Class I device made by Richard Wolf GmbH, registered in EUDAMED on 1 Sep 2026 (Basic UDI-DI B-04055207038734) and listed in FDA GUDID since 28 Sep 2016 (UDI-DI 04055207038734), 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-04055207038734 Basic UDI-DI 04055207038734UDI-DIDate1 Sep 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number04055207038734 UDI-DI Date28 Sep 2016ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI B-04055207038734 registered 1 Sep 2026 Active
  • FDA GUDID UDI-DI 04055207038734 listed 28 Sep 2016 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 04055207038734
  2. Registered EUDAMED B-04055207038734

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  • Withdrawn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 biopsy forceps, reusable
Device name
Flex. bronch. grasping/biopsy forceps
Model / Ref / Catalog
10000201282, 7223.60, 722360
Description
FLEX. BIOPSY FORCEPS Ø 1MM WL 600MM smooth, double opening, TL 736mm, reusable
Primary DI / UDI-DI
04055207038734
Basic UDI-DI
B-04055207038734
FDA product code
KAE, GEN
EMDN code
L080899 Bronchoscopic surgery instruments, reusable - other
GMDN term
Flexible endoscopic biopsy forceps, reusable
Device class
Class I
Regulation number
874.4420, 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 — 600 Millimeter
Outer Diameter — 1 Millimeter

Truth per registry

2 sources · 1 field differs

FieldEUDAMEDGUDID
Model / referenceEUDAMED
10000201282
7223.60
GUDID
722360

Related devices

Category: Flexible endoscopic biopsy forceps, reusable

Similar devices in this category

Other devices filed under THORACIC 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)