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Aesculap AN909R

by Aesculap AG

Part of a family of 14 devices: see the family page

Ref AN909R

Aesculap AN909R is a Class I device made by Aesculap AG, registered in EUDAMED on 22 Sep 2026 (Basic UDI-DI 40392390000004772N) and listed in FDA GUDID since 2 Jul 2020 (UDI-DI 04038653019519), 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 Number40392390000004772N Basic UDI-DI 04038653019519UDI-DIDate22 Sep 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number04038653019519 UDI-DI Date2 Jul 2020ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI 40392390000004772N registered 22 Sep 2026 Active
  • FDA GUDID UDI-DI 04038653019519 listed 2 Jul 2020 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 04038653019519
  2. Registered EUDAMED 40392390000004772N

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  • Withdrawn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
Dressing/utility forceps, scissors-like, reusable
Device name
Material clamp I
Model / Ref / Catalog
AN909R
Primary DI / UDI-DI
04038653019519
Basic UDI-DI
40392390000004772N
Direct marketing DI
04038653019519
FDA product code
HXD
EMDN code
L031307 Towel and tube clamps, reusable
GMDN term
Dressing/utility forceps, scissors-like, 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: Dressing/utility forceps, scissors-like, reusable

Similar devices in this category

Other devices filed under GENERAL SURGERY FORCEPS, REUSABLE.

Other devices from Aesculap AG

See all devices from Aesculap AG →

Properties

  • Sterilise before use
  • Prescription use
  • Premarket exempt
  • Lot / batch number
Other properties (21, all answered No)