← Back to catalogue

Maia Rasp S7s

EUDAMED

Class I (EU MDR)

Ref M100 5117Model Class Ir Instrument

by groupe lépine

Identity

Trade Name
MAIA RASP S7S EUDAMED
Device Name
Class Ir Instrument EUDAMED
Model / Reference
Class Ir Instrument EUDAMED
M100 5117 EUDAMED

Identifiers

Primary DI / UDI-DI
+M483M10051170 EUDAMED
Basic UDI-DI
++M483L0912YQ EUDAMED
Direct Marketing DI
+M483M10051170 EUDAMED
EMDN Code
L091201 ORTHOPAEDIC SURGERY RASPS, REUSABLE EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
France EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Implantable

No

EUDAMED

Reusable

Yes

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

Maia Rasp S7s by groupe lépine — Class I — MDR — listed in EUDAMED — regulatory data on deviCERTS

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

Manufacturer
groupe lépine
EUDAMED SRN
FR-MF-000001182

Sources (1)

  • EUDAMED d034e893-a934-4b67-b675-2362c01a1f98 61 fields · synced Jul 15, 2026