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Aesculap

by Aesculap AG 1,000+ variants

Part of a family of 19 devices: see the family page

Ref ME619R

Aesculap (ME619R) is a Class I device made by Aesculap AG, registered in EUDAMED on 18 Nov 2025 (Basic UDI-DI 4039239000000305ZM) and listed in FDA GUDID since 24 Apr 2020 (UDI-DI 04046963975593), active (EUDAMED), not in commercial distribution (GUDID) as of 22 Oct 2026.

Active European Union. Also listed in GUDID (US), not in commercial distribution.

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 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR EUDAMED Number4039239000000305ZM Basic UDI-DI 04046963975593UDI-DIDate18 Nov 2025RegisteredStatusActive
United StatesGUDID listing GUDID Number04046963975593 UDI-DI Date24 Apr 2020ListedStatusListed GUDID: not in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI 4039239000000305ZM registered 18 Nov 2025 Active
  • FDA GUDID UDI-DI 04046963975593 listed 24 Apr 2020 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 04046963975593
  2. Registered EUDAMED 4039239000000305ZM

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  • Withdrawn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 EUDAMED
A-Space Sibd GUDID
Generic name
Bone curette, reusable
Device name
ARCADIUS XP L dissection instrument
Model / Ref / Catalog
ME619R
Primary DI / UDI-DI
04046963975593
Basic UDI-DI
4039239000000305ZM
Direct marketing DI
04046963975593
FDA product code
HTF
EMDN code
L091099 Osteosynthesis instruments, reusable - other
GMDN term
Bone curette, reusable
Device class
Class I
Regulation number
878.4800
EU registration type
Standard device
EU market of registration
Germany
GUDID distribution status
Not in Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

Manufacturer details

EUDAMED SRN
DE-MF-000005504

Related devices

Category: Surgical implant template, reusable

Similar devices in this category

Other devices filed under OSTEOSYNTHESIS INSTRUMENTS, REUSABLE - OTHER.

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)