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devemed 522 P

by devemed GmbH

Part of a family of 542 devices: see the family page

Ref 522 P

devemed 522 P is a Class I device made by devemed GmbH, registered in EUDAMED on 10 Jul 2026 (Basic UDI-DI 4061644PG0202CC) and listed in FDA GUDID since 23 Apr 2020 (UDI-DI 04061644007097), 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 Number4061644PG0202CC Basic UDI-DI 04061644007097UDI-DIDate10 Jul 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number04061644007097 UDI-DI Date23 Apr 2020ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI 4061644PG0202CC registered 10 Jul 2026 Active
  • FDA GUDID UDI-DI 04061644007097 listed 23 Apr 2020 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 04061644007097
  2. Registered EUDAMED 4061644PG0202CC

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  • Withdrawn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
Tooth extraction forceps
Model / reference
522 P
Description
SPECIAL-EXTRACT - Extracting forceps Molars
Primary DI / UDI-DI
04061644007097
Basic UDI-DI
4061644PG0202CC
Direct marketing DI
04061644007097
FDA product code
EMG
EMDN code
L150301 Dental extraction tooth forceps, reusable
GMDN term
Tooth extraction forceps
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: Tooth extraction forceps

Similar devices in this category

Other devices filed under DENTAL EXTRACTION TOOTH FORCEPS, 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)