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FlexMaster®

EUDAMED

Class IIa (EU MDR)

Ref V040341025035

by Maillefer Instruments Holding Sàrl

Identity

Trade Name
FlexMaster® EUDAMED
Device Name
FlexMaster® EUDAMED
Model / Reference
V040341025035 EUDAMED

Identifiers

Primary DI / UDI-DI
+J003V0403410250351 EUDAMED
Basic UDI-DI
++J00310145E8 EUDAMED
Unit of Use DI
+J003V0403410250350 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

FlexMaster® by Maillefer Instruments Holding Sàrl — Class IIa — 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
CH-MF-000016301
Authorised Representative
Dentsply DeTrey GmbH DE-AR-000005904

Sources (1)

  • EUDAMED aacaf2f9-cc9a-4662-9b45-fda4f5b95e3f 61 fields · synced Jul 21, 2026