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Aesculap BH018R

by Aesculap, Inc.

Part of a family of 62 devices: see the family page

Ref BH018R

Aesculap BH018R is a Class I device made by Aesculap, Inc., registered in EUDAMED on 22 Sep 2026 (Basic UDI-DI 40392390000004552C) and listed in FDA GUDID since 7 Jul 2020 (UDI-DI 04038653025473), active as of 23 Oct 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 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR EUDAMED Number40392390000004552C Basic UDI-DI 04038653025473UDI-DIDate22 Sep 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number04038653025473 UDI-DI Date7 Jul 2020ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI 40392390000004552C registered 22 Sep 2026 Active
  • FDA GUDID UDI-DI 04038653025473 listed 7 Jul 2020 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 04038653025473
  2. Registered EUDAMED 40392390000004552C

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  • Withdrawn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
Open-surgery ligation clip applier
Device name
Bulldog clamp
Model / Ref / Catalog
BH018R
Primary DI / UDI-DI
04038653025473
Basic UDI-DI
40392390000004552C
Direct marketing DI
04038653025473
FDA product code
HTD
EMDN code
L070801018001 Forceps for the application and removal of vascular clips, reusable
GMDN term
Open-surgery ligation clip applier
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

Related devices

Category: Open-surgery ligation clip applier

Similar devices in this category

Other devices filed under CARDIOVASCULAR SURGERY INSTRUMENTS, REUSABLE.

Other devices from Aesculap, Inc.

See all devices from Aesculap, Inc. →

Properties

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