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Re-Force

EUDAMED

Class I (EU MDR)

Ref M01682

by Polydentia SA

Identity

Trade Name
Re-Force EUDAMED
Device Name
DENTAL RINGS EUDAMED
Model / Reference
M01682 EUDAMED

Identifiers

Primary DI / UDI-DI
+E299M016820 EUDAMED
Basic UDI-DI
++E299DENTALRINGSM6 EUDAMED
EMDN Code
Q01010199 DENTAL RESTORATION DEVICES - OTHER EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Liechtenstein EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Implantable

No

EUDAMED

Reusable

No

EUDAMED

Contains Latex

No

EUDAMED

Reprocessed

No

EUDAMED

CMR Substance

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Endocrine Disruptor

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

Category: Dental appliance fabrication material, ceramic

Re-Force by Polydentia SA — Class I — MDR — listed in EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Dental appliance fabrication material, ceramic.

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

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Manufacturer

Manufacturer
Polydentia SA
EUDAMED SRN
CH-MF-000008779
Authorised Representative
IDD International Dental Distributors AG LI-AR-000008367

Sources (1)

  • EUDAMED 80f2f0ca-4a30-43f9-a5ff-4ab4ae877e4d 61 fields · synced Jun 19, 2026