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FlexMaster®

EUDAMED

Class IIa (EU MDR)

Ref V040341025050

by Maillefer Instruments Holding Sàrl

Identity

Trade Name
FlexMaster® EUDAMED
Device Name
FlexMaster® EUDAMED
Model / Reference
V040341025050 EUDAMED

Identifiers

Primary DI / UDI-DI
+J003V0403410250501 EUDAMED
Basic UDI-DI
++J00310145E8 EUDAMED
Unit of Use DI
+J003V0403410250500 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

FlexMaster® 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

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Manufacturer

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

Sources (1)

  • EUDAMED 0a9862c6-d47f-4757-8e1f-58cdf41117b0 61 fields · synced Jul 19, 2026