Skip to content

Aesculap DP101R

by Aesculap, Inc.

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

Ref DP101R

Aesculap DP101R is a Class I device made by Aesculap, Inc., registered in EUDAMED on 28 Aug 2025 (Basic UDI-DI 4039239000000510ZQ) and listed in FDA GUDID since 20 Apr 2020 (UDI-DI 04038653037865), active as of 23 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 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR EUDAMED Number4039239000000510ZQ Basic UDI-DI 04038653037865UDI-DIDate28 Aug 2025RegisteredStatusActive
United StatesGUDID listing GUDID Number04038653037865 UDI-DI Date20 Apr 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 04038653037865 listed 20 Apr 2020 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 04038653037865
  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  • Withdrawn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

Trade name
Aesculap
Generic name
Orthodontic pliers
Device name
Technical forceps dental
Model / Ref / Catalog
DP101R
Primary DI / UDI-DI
04038653037865
Basic UDI-DI
4039239000000510ZQ
Direct marketing DI
04038653037865
FDA product code
EJY
EMDN code
L150702 Orthodontic pliers, reusable
GMDN term
Orthodontic pliers
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

Similar devices in this category

Other devices filed under ORTHODONTIC PLIERS, REUSABLE.

Other devices from Aesculap, Inc.

See all devices from Aesculap, Inc. →

Properties

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