Skip to content

Aesculap DE052R

by Aesculap, Inc.

Part of a family of 59 devices: see the family page

Ref DE052R

Aesculap DE052R is a Class I device made by Aesculap, Inc., registered in EUDAMED on 25 Sep 2025 (Basic UDI-DI 403923900000055027) and listed in FDA GUDID since 17 Jun 2020 (UDI-DI 04038653242597), 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 Number403923900000055027 Basic UDI-DI 04038653242597UDI-DIDate25 Sep 2025RegisteredStatusActive
United StatesGUDID listing GUDID Number04038653242597 UDI-DI Date17 Jun 2020ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI 403923900000055027 registered 25 Sep 2025 Active
  • FDA GUDID UDI-DI 04038653242597 listed 17 Jun 2020 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 04038653242597
  2. Registered EUDAMED 403923900000055027

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  • Withdrawn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
Dental spatula, reusable
Device name
Dental filling instruments
Model / Ref / Catalog
DE052R
Primary DI / UDI-DI
04038653242597
Basic UDI-DI
403923900000055027
FDA product code
EKG
EMDN code
L1504 Odontostomatology modelers, reusable
GMDN term
Dental spatula, 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

Related devices

Category: Dental spatula, 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)