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Atraumata FB382R

by Aesculap, Inc.

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

Ref FB382R

Atraumata FB382R 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 23 Apr 2020 (UDI-DI 04046963457792), active as of 24 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 24 Oct 2026.

Regulatory status

as of registry sync 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR EUDAMED Number40392390000004552C Basic UDI-DI 04046963457792UDI-DIDate22 Sep 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number04046963457792 UDI-DI Date23 Apr 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 04046963457792 listed 23 Apr 2020 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 04046963457792
  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  • Withdrawn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
Atraumata® EUDAMED
Atraumata GUDID
Generic name
Surgical bulldog clamp, reusable
Model / Ref / Catalog
FB382R
Primary DI / UDI-DI
04046963457792
Basic UDI-DI
40392390000004552C
Direct marketing DI
04046963457792
FDA product code
HXD
EMDN code
L0708010101 Bulldog vascular clips, reusable
GMDN term
Surgical bulldog clamp, reusable
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: Surgical bulldog clamp, reusable

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)