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Aesculap DB939R

by Aesculap, Inc.

Ref DB939R

Aesculap DB939R is a Class I device made by Aesculap, Inc., registered in EUDAMED on 16 Sep 2025 (Basic UDI-DI 40392390000017893K) and listed in FDA GUDID since 17 Jun 2020 (UDI-DI 04038653147687), 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 Number40392390000017893K Basic UDI-DI 04038653147687UDI-DIDate16 Sep 2025RegisteredStatusActive
United StatesGUDID listing GUDID Number04038653147687 UDI-DI Date17 Jun 2020ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI 40392390000017893K registered 16 Sep 2025 Active
  • FDA GUDID UDI-DI 04038653147687 listed 17 Jun 2020 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 04038653147687
  2. Registered EUDAMED 40392390000017893K

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  • Withdrawn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
Periodontal knife
Device name
Dental knife
Model / Ref / Catalog
DB939R
Primary DI / UDI-DI
04038653147687
Basic UDI-DI
40392390000017893K
Direct marketing DI
04038653147687
FDA product code
EMO
EMDN code
L010101 Monoblock surgical scalpels, reusable
GMDN term
Periodontal knife
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 MONOBLOCK SURGICAL SCALPELS, REUSABLE.

Other devices from Aesculap, Inc.

See all devices from Aesculap, Inc. →

Properties

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