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devemed 2500-19 F

by devemed GmbH

Ref 2500-19 F

devemed 2500-19 F is a Class I device made by devemed GmbH, registered in EUDAMED on 7 Jul 2026 (Basic UDI-DI 4061644PG010202034V) and listed in FDA GUDID since 21 Apr 2020 (UDI-DI 04061644022519), active as of 24 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 24 Oct 2026.

Regulatory status

as of registry sync 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR EUDAMED Number4061644PG010202034V Basic UDI-DI 04061644022519UDI-DIDate7 Jul 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number04061644022519 UDI-DI Date21 Apr 2020ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI 4061644PG010202034V registered 7 Jul 2026 Active
  • FDA GUDID UDI-DI 04061644022519 listed 21 Apr 2020 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 04061644022519
  2. Registered EUDAMED 4061644PG010202034V

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  • Withdrawn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
devemed
Generic name
Periotome, reusable
Device name
Periotomes
Model / reference
2500-19 F
Description
Periotome 2.0 mm, straigth / bent over surface F-LINE | SL | double ended
Primary DI / UDI-DI
04061644022519
Basic UDI-DI
4061644PG010202034V
Direct marketing DI
04061644022519
FDA product code
EKD
EMDN code
L0102 Surgical knives, reusable
GMDN term
Periotome, 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: Periotome, reusable

Other devices from devemed GmbH

See all devices from devemed GmbH →

Properties

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