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Aesculap SJ708T

by Aesculap AG

Part of a family of 6 devices: see the family page

Ref SJ708T

Aesculap SJ708T is a Class I device made by Aesculap AG, registered in EUDAMED on 25 Sep 2025 (Basic UDI-DI 4039239000000303ZH) and listed in FDA GUDID since 24 Apr 2020 (UDI-DI 04046964061141), active (EUDAMED), not in commercial distribution (GUDID) as of 12 Nov 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 12 Nov 2026.

Regulatory status

as of registry sync 12 Nov 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR EUDAMED Number4039239000000303ZH Basic UDI-DI 04046964061141UDI-DIDate25 Sep 2025RegisteredStatusActive
United StatesGUDID listing GUDID Number04046964061141 UDI-DI Date24 Apr 2020ListedStatusListed GUDID: not in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI 4039239000000303ZH registered 25 Sep 2025 Active
  • FDA GUDID UDI-DI 04046964061141 listed 24 Apr 2020 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 04046964061141
  2. Registered EUDAMED 4039239000000303ZH

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  • Withdrawn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
Orthopaedic prosthesis implantation positioning instrument, reusable
Device name
ARCADIUS XP L implant. instrument I
Model / Ref / Catalog
SJ708T
Primary DI / UDI-DI
04046964061141
Basic UDI-DI
4039239000000303ZH
Direct marketing DI
04046964061141
FDA product code
LXH
EMDN code
L0903 Orthopaedic surgery hammers, reusable
GMDN term
Orthopaedic prosthesis implantation positioning instrument, reusable
Device class
Class I
Regulation number
888.4540
EU registration type
Standard device
EU market of registration
Germany
GUDID distribution status
Not in Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

Similar devices in this category

Other devices filed under ORTHOPAEDIC SURGERY HAMMERS, REUSABLE.

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Properties

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