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Re-Force

by Polydentia SA

Part of a family of 37 devices: see the family page

Ref M01682

Re-Force (M01682) is a Class I device made by Polydentia SA, registered in EUDAMED on 8 Nov 2021 (Basic UDI-DI ++E299DENTALRINGSM6), active as of 23 Oct 2026.

Active European Union

CE MDR

Valid until

No date given

EUDAMED holds no validity date

FDA recalls

Not applicable

No FDA record for this device

Documents

None, self-declared

Class I: no certifier involved

Trust

Unverified

Source EUDAMED, synced 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number++E299DENTALRINGSM6 Basic UDI-DI +E299M016820UDI-DIDate8 Nov 2021RegisteredStatusActive

Official records

Certificates

0 certificates · EUDAMED

No certifier certificate is listed. Devices of this class are self-declared by the manufacturer.

Coverage

1 jurisdiction

SwedenFinlandLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaAustriaHungaryRomaniaSloveniaBulgariaPortugalSpainItalyCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

European Union — CE/MDR Active

Specification

EUDAMED

Device name
Dental Rings
Model / reference
M01682
Primary DI / UDI-DI
+E299M016820
Basic UDI-DI
++E299DENTALRINGSM6
EMDN code
Q01010199 Dental restoration devices - other
Device class
Class I
EU registration type
Standard device
EU market of registration
Liechtenstein

Manufacturer details

EUDAMED SRN
CH-MF-000008779
Authorised representative
IDD International Dental Distributors AG LI-AR-000008367

Related devices

Category: Dental appliance fabrication material, ceramic

Similar devices in this category

Other devices filed under DENTAL RESTORATION DEVICES - OTHER.

Other devices from Polydentia SA

See all devices from Polydentia SA →

Properties

  • Sterilise before use
Other properties (13, all answered No)