8243604

by Richard Wolf GmbH

Ref 8243.604Model 10000201425

8243604 (8243.604) is a Class I device made by Richard Wolf GmbH, registered in EUDAMED on 7 Sep 2026 (Basic UDI-DI B-04055207014721) and listed in FDA GUDID since 9 Aug 2022 (UDI-DI 04055207014721), 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

Source EUDAMED, GUDID, synced 24 Oct 2026.

Regulatory status

as of registry sync 24 Oct 2026

Region	Authorization	Number	Date	Status
European Union	CE/MDD EUDAMED	NumberB-04055207014721 Basic UDI-DI 04055207014721UDI-DI	Date7 Sep 2026Registered	StatusActive
United States	GUDID listing GUDID	Number04055207014721 UDI-DI	Date9 Aug 2022Listed	StatusListed GUDID: in commercial distribution

Official records

EUDAMED public site Basic UDI-DI B-04055207014721 — open Devices and search for it
AccessGUDID record UDI-DI 04055207014721

Across registries

2 registries list this device

EUDAMED Basic UDI-DI B-04055207014721 registered 7 Sep 2026 Active
FDA GUDID UDI-DI 04055207014721 listed 9 Aug 2022 Listed

Timeline

2 dated events

9 Aug 2022 Listed FDA GUDID 04055207014721
7 Sep 2026 Registered EUDAMED B-04055207014721

Coverage

2 jurisdictions

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Withdrawn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: Thoracoscopic grasping forceps
Model / Ref / Catalog: 10000201425, 8243.604, 8243604
Description: PARENCHYM GRASP. FORCEPS Ø 7MM WL 264MM jaw straight, sheath curved upwards, TL 396mm, reusable

Primary DI / UDI-DI: 04055207014721
Basic UDI-DI: B-04055207014721
FDA product code: GEN
EMDN code: L080599 Thoracic surgery clamps, reusable - other
GMDN term: Rigid endoscopic tissue manipulation forceps, 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: Outer Diameter — 7 Millimeter
Length — 264 Millimeter

Truth per registry

2 sources · 1 field differs

Field	EUDAMED	GUDID
Model / reference	EUDAMED 10000201425 8243.604	GUDID 8243604

Similar devices in this category

Other devices filed under THORACIC SURGERY FORCEPS, REUSABLE.

Other devices from Richard Wolf GmbH

Arthroscopic compactors

Class I
Insufflators

Class IIb
Modular sheath tubes for needle holders

Class I
Colpotransilluminators with vacuum tube

Class IIa

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)