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Prophy Cup

EUDAMED

Class I (EU MDR)

Ref 252RModel 252R, 252S, 252RA, 252SA,252RB, 252SG

by Rocodent International Limited

Identity

Device Name
Prophy Cup EUDAMED
Model / Reference
252R, 252S, 252RA, 252SA,252RB, 252SG EUDAMED
252R EUDAMED

Identifiers

Primary DI / UDI-DI
06975336240168 EUDAMED
Basic UDI-DI
697533624RPC005M3 EUDAMED
EMDN Code
Q010502 DENTAL POLISHING CUPS, SINGLE-USE EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Austria 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: Dentifrice

Prophy Cup by Rocodent International Limited — Class I — MDR — listed in EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Dentifrice.

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

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Manufacturer

EUDAMED SRN
CN-MF-000045441
Authorised Representative
SUNGO Europe B.V. NL-AR-000000247

Sources (1)

  • EUDAMED d5508583-760e-42bd-97f4-fc6254496f0c 61 fields · synced Jun 19, 2026