← Back to catalogue

Vdw.rotate®

EUDAMED

Class IIa (EU MDR)

Ref MSTVROT331AST

by Maillefer Instruments Holding Sàrl

Identity

Trade Name
VDW.ROTATE® EUDAMED
Device Name
VDW.ROTATE® EUDAMED
Model / Reference
MSTVROT331AST EUDAMED

Identifiers

Primary DI / UDI-DI
+J003MSTVROT331AST1 EUDAMED
Basic UDI-DI
++J00310149EG EUDAMED
Unit of Use DI
+J003MSTVROT331AST0 EUDAMED
EMDN Code
L159004 ENDODONTIC RASPS AND FILES, REUSABLE EUDAMED

Classification

Device Class
Class IIa EUDAMED
Market of Registration
Austria EUDAMED

Clinical & Handling

Sterile

Yes

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: Manual endodontic file/rasp, reusable

Vdw.rotate® by Maillefer Instruments Holding Sàrl — Class IIa — MDR — listed in EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Manual endodontic file/rasp, reusable.

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

Is this your device? Claim it to add documentation and request validation.

Manufacturer

EUDAMED SRN
CH-MF-000016301
Authorised Representative
Dentsply DeTrey GmbH DE-AR-000005904

Sources (1)

  • EUDAMED 75dff9de-c5b7-46d8-a73d-7581187bfbca 61 fields · synced Jul 29, 2026