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Aesculap

by Aesculap AG 1,000+ variants

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

Ref DP150R

Aesculap (DP150R) is a Class I device made by Aesculap AG, registered in EUDAMED on 25 Sep 2025 (Basic UDI-DI 403923900000054024) and listed in FDA GUDID since 20 Apr 2020 (UDI-DI 04038653037957), 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 Number403923900000054024 Basic UDI-DI 04038653037957UDI-DIDate25 Sep 2025RegisteredStatusActive
United StatesGUDID listing GUDID Number04038653037957 UDI-DI Date20 Apr 2020ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI 403923900000054024 registered 25 Sep 2025 Active
  • FDA GUDID UDI-DI 04038653037957 listed 20 Apr 2020 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 04038653037957
  2. Registered EUDAMED 403923900000054024

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  • Withdrawn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
Surgical soft-tissue manipulation forceps, tweezers-like, reusable
Device name
Tweezers I
Model / Ref / Catalog
DP150R
Primary DI / UDI-DI
04038653037957
Basic UDI-DI
403923900000054024
Direct marketing DI
04038653037957
FDA product code
EMG
EMDN code
L150702 Orthodontic pliers, reusable
GMDN term
Surgical soft-tissue manipulation forceps, tweezers-like, reusable
Device class
Class I
Regulation number
872.4565
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)