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8756201

by Richard Wolf GmbH

Ref 8756.201Model 10000201326

8756201 (8756.201) is a Class I device made by Richard Wolf GmbH, registered in EUDAMED on 6 Oct 2026 (Basic UDI-DI B-04055207020494) and listed in FDA GUDID since 8 Dec 2022 (UDI-DI 04055207020494), 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-04055207020494 Basic UDI-DI 04055207020494UDI-DIDate6 Oct 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number04055207020494 UDI-DI Date8 Dec 2022ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI B-04055207020494 registered 6 Oct 2026 Active
  • FDA GUDID UDI-DI 04055207020494 listed 8 Dec 2022 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 04055207020494
  2. Registered EUDAMED B-04055207020494

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  • Withdrawn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
Suturing unit, reusable
Device name
Surgical laparoscopic needle forceps
Model / Ref / Catalog
10000201326, 8756.201, 8756201
Description
NEEDLE FORCEPS Ø 2.45MM WL 160MM with single action jaw to carry suture diamèter 2 mm, WL 160 mm
Primary DI / UDI-DI
04055207020494
Basic UDI-DI
B-04055207020494
FDA product code
GEN
EMDN code
L0299 Suture instruments, reusable - other
GMDN term
Suturing unit, reusable
Device class
Class I
Regulation number
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 — 160 Millimeter
Outer Diameter — 2.45 Millimeter

Truth per registry

2 sources · 1 field differs

FieldEUDAMEDGUDID
Model / referenceEUDAMED
10000201326
8756.201
GUDID
8756201

Related devices

Category: Suturing unit, reusable

Similar devices in this category

Other devices filed under SUTURE 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)