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Aesculap FB282R

by Aesculap AG

Ref FB282R

Aesculap FB282R is a Class I device made by Aesculap AG, registered in EUDAMED on 13 Oct 2025 (Basic UDI-DI 403923900000068835) and listed in FDA GUDID since 24 Apr 2020 (UDI-DI 04046964071904), 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 Number403923900000068835 Basic UDI-DI 04046964071904UDI-DIDate13 Oct 2025RegisteredStatusActive
United StatesGUDID listing GUDID Number04046964071904 UDI-DI Date24 Apr 2020ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI 403923900000068835 registered 13 Oct 2025 Active
  • FDA GUDID UDI-DI 04046964071904 listed 24 Apr 2020 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 04046964071904
  2. Registered EUDAMED 403923900000068835

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  • Withdrawn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
Skin staple remover, reusable
Device name
Ligatur clip remover
Model / Ref / Catalog
FB282R
Primary DI / UDI-DI
04046964071904
Basic UDI-DI
403923900000068835
Direct marketing DI
04046964071904
FDA product code
GDO
EMDN code
H03010105 Reusable multiple clip applier cartridges for open surgery
GMDN term
Skin staple remover, 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

Similar devices in this category

Other devices filed under HAEMOSTASIS CLIPS FOR OPEN SURGERY.

Other devices from Aesculap AG

See all devices from Aesculap AG →

Properties

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