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Aesculap

by Aesculap AG 1,000+ variants

Part of a family of 44 devices: see the family page

Ref DP520R

Aesculap (DP520R) is a Class I device made by Aesculap AG, registered in EUDAMED on 28 Aug 2025 (Basic UDI-DI 4039239000000510ZQ) and listed in FDA GUDID since 10 Aug 2020 (UDI-DI 04038653038268), active as of 22 Oct 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 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR EUDAMED Number4039239000000510ZQ Basic UDI-DI 04038653038268UDI-DIDate28 Aug 2025RegisteredStatusActive
United StatesGUDID listing GUDID Number04038653038268 UDI-DI Date10 Aug 2020ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI 4039239000000510ZQ registered 28 Aug 2025 Active
  • FDA GUDID UDI-DI 04038653038268 listed 10 Aug 2020 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 04038653038268
  2. Registered EUDAMED 4039239000000510ZQ

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  • Withdrawn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

Generic name
Orthopaedic implantable-device cutter
Device name
Technical forceps dental
Model / Ref / Catalog
DP520R
Primary DI / UDI-DI
04038653038268
Basic UDI-DI
4039239000000510ZQ
Direct marketing DI
04038653038268
FDA product code
HXZ
EMDN code
L150702 Orthodontic pliers, reusable
GMDN term
Orthopaedic implantable-device cutter
Device class
Class I
Regulation number
888.4540
EU registration type
Standard device
EU market of registration
Germany
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

Manufacturer details

EUDAMED SRN
DE-MF-000005504

Similar devices in this category

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Properties

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