Skip to content

Stoma® 822.00

by Storz am Mark GmbH

Part of a family of 99 devices: see the family page

Ref 822.00Model 35552 - Tooth extraction forceps (029)

Stoma® 822.00 is a Class I device made by Storz am Mark GmbH, registered in EUDAMED on 5 Oct 2026 (Basic UDI-DI ++ESAM02994) and listed in FDA GUDID since 27 Aug 2020 (UDI-DI +ESAM822001), active as of 25 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 25 Oct 2026.

Regulatory status

as of registry sync 25 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR EUDAMED Number++ESAM02994 Basic UDI-DI +ESAM822001UDI-DIDate5 Oct 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number+ESAM822001 UDI-DI Date27 Aug 2020ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI ++ESAM02994 registered 5 Oct 2026 Active
  • FDA GUDID UDI-DI +ESAM822001 listed 27 Aug 2020 Listed

Timeline

2 dated events

  1. Listed FDA GUDID +ESAM822001
  2. Registered EUDAMED ++ESAM02994

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  • Withdrawn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
UK Molaren, HP, Fig. 22, Fifo EUDAMED
Stoma® GUDID
Generic name
Tooth extraction forceps
Model / Ref / Catalog
822.00, 35552 - Tooth extraction forceps (029)
Primary DI / UDI-DI
+ESAM822001 EUDAMED
ESAM822001 GUDID
Basic UDI-DI
++ESAM02994
Direct marketing DI
+ESAM822000
FDA product code
EMG
EMDN code
L150101 Odontostomatology osteotomes, 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

Truth per registry

2 sources · 1 field differs

FieldEUDAMEDGUDID
Primary DI / UDI-DIEUDAMED
+ESAM822001
GUDID
ESAM822001

The registries describe this device under different primary UDI-DIs (EUDAMED lists +ESAM822001; FDA GUDID lists ESAM822001), so their flags are not compared.

Related devices

Category: Tooth extraction forceps

Similar devices in this category

Other devices filed under ODONTOSTOMATOLOGY OSTEOTOMES, REUSABLE.

Other devices from Storz am Mark GmbH

See all devices from Storz am Mark GmbH →

Properties

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