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Aesculap BV941R

by Aesculap AG

Ref BV941R

Aesculap BV941R is a stone/foreign-body extraction set (EU MDR Class I; FDA Class I; FDA product code GAD, Retractor) made by Aesculap AG, registered in EUDAMED on 18 Nov 2025 (Basic UDI-DI 40392390000016502K) and listed in FDA GUDID since 4 May 2020 (UDI-DI 04038653032808), active as of 12 Nov 2026.

Active European Union. Also listed in GUDID (US).

CE MDR

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 12 Nov 2026.

Regulatory status

as of registry sync 12 Nov 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR EUDAMED Number40392390000016502K Basic UDI-DI 04038653032808UDI-DIDate18 Nov 2025RegisteredStatusActive
United StatesGUDID listing GUDID Number04038653032808 UDI-DI Date4 May 2020ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI 40392390000016502K registered 18 Nov 2025 Active
  • FDA GUDID UDI-DI 04038653032808 listed 4 May 2020 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 04038653032808
  2. Registered EUDAMED 40392390000016502K

Coverage

2 jurisdictions

United States of AmericaSwedenFinlandLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaAustriaHungaryRomaniaSloveniaBulgariaPortugalSpainItalyCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered
  • European Union CE/MDR Active
  • United States GUDID listing Listed

Specification

EUDAMED · GUDID

Trade name
Aesculap
Generic name
Stone/foreign-body extraction set
Device name
Gallbladder extractor
Model / Ref / Catalog
BV941R
Primary DI / UDI-DI
04038653032808
Basic UDI-DI
40392390000016502K
Direct marketing DI
04038653032808
FDA product code
GAD
EMDN code
L04080101 Gallbladder forceps, reusable
GMDN term
Stone/foreign-body extraction set
Device class
Class I
Regulation number
878.4800
EU registration type
Standard device
EU market of registration
Germany
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

Similar devices in this category

Other devices filed under ABDOMINAL SURGERY INSTRUMENTS, REUSABLE.

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Properties

  • Sterilise before use
  • Reusable
  • Prescription use
  • Premarket exempt
  • Lot / batch number
Other properties (20, all answered No)