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Prophy brush

EUDAMED

Class I (EU MDR)

Ref 262FModel 262F, 262T, 268N, 268B, 268NA, 262FA, 262TA, 263,265, 269

by Rocodent International Limited

Identity

Device Name
Prophy brush EUDAMED
Model / Reference
262F, 262T, 268N, 268B, 268NA, 262FA, 262TA, 263,265, 269 EUDAMED
262F EUDAMED

Identifiers

Primary DI / UDI-DI
06975336240069 EUDAMED
Basic UDI-DI
697533624RPB004LS EUDAMED
EMDN Code
Q01010403 DENTAL ABRASIVE AND POLISHING MATERIALS 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

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

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 3512b62f-ac84-43b1-89f2-4a3a49fbc9b7 61 fields · synced Jun 18, 2026