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Aesculap

by Aesculap AG 1,000+ variants

Ref DP725R

Aesculap (DP725R) is a Class I device made by Aesculap AG, registered in EUDAMED on 13 Oct 2025 (Basic UDI-DI 40392390000005872W) and listed in FDA GUDID since 7 May 2020 (UDI-DI 04038653038367), 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 Number40392390000005872W Basic UDI-DI 04038653038367UDI-DIDate13 Oct 2025RegisteredStatusActive
United StatesGUDID listing GUDID Number04038653038367 UDI-DI Date7 May 2020ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI 40392390000005872W registered 13 Oct 2025 Active
  • FDA GUDID UDI-DI 04038653038367 listed 7 May 2020 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 04038653038367
  2. Registered EUDAMED 40392390000005872W

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  • Withdrawn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
Dental/maxillofacial surgical procedure kit, non-medicated, reusable
Device name
Caliper
Model / Ref / Catalog
DP725R
Primary DI / UDI-DI
04038653038367
Basic UDI-DI
40392390000005872W
Direct marketing DI
04038653038367
FDA product code
DZN
EMDN code
V0399 Measurement devices - other
GMDN term
Dental/maxillofacial surgical procedure kit, non-medicated, 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

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Other devices filed under MEASUREMENT DEVICES - OTHER.

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Properties

  • Sterilise before use
  • Reusable
  • Over-the-counter
  • Premarket exempt
  • Lot / batch number
Other properties (20, all answered No)