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Aesculap NP743R

by Aesculap AG

Ref NP743R

Aesculap NP743R is a Class I device made by Aesculap AG, registered in EUDAMED on 11 Aug 2026 (Basic UDI-DI 40392390000018673E) and listed in FDA GUDID since 23 Apr 2020 (UDI-DI 04038653296057), 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 Number40392390000018673E Basic UDI-DI 04038653296057UDI-DIDate11 Aug 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number04038653296057 UDI-DI Date23 Apr 2020ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI 40392390000018673E registered 11 Aug 2026 Active
  • FDA GUDID UDI-DI 04038653296057 listed 23 Apr 2020 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 04038653296057
  2. Registered EUDAMED 40392390000018673E

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  • Withdrawn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
Implantation instrument TKA Ir
Model / Ref / Catalog
NP743R
Primary DI / UDI-DI
04038653296057
Basic UDI-DI
40392390000018673E
Direct marketing DI
04038653296057
FDA product code
HTD
EMDN code
L091199 Orthopaedic prosthetics instruments, reusable - other
GMDN term
Orthopaedic prosthesis implantation positioning instrument, 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: Orthopaedic prosthesis implantation positioning instrument, reusable

Similar devices in this category

Other devices filed under ORTHOPAEDIC PROSTHETICS 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)