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Sliding Extramedullary Rod

EUDAMED

Class I (EU MDR)

Ref G101 6150Model Class I Instrument

by groupe lépine

Identity

Trade Name
SLIDING EXTRAMEDULLARY ROD EUDAMED
Device Name
Class I Instrument EUDAMED
Model / Reference
Class I Instrument EUDAMED
G101 6150 EUDAMED

Identifiers

Primary DI / UDI-DI
+M483G10161500 EUDAMED
Basic UDI-DI
++M483L0999ZW EUDAMED
Direct Marketing DI
+M483G10161500 EUDAMED
EMDN Code
L0999 ORTHOPAEDIC AND TRAUMATOLOGICAL SURGERY INSTRUMENTS, REUSABLE - OTHER 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

Sliding Extramedullary Rod 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

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Manufacturer

Manufacturer
groupe lépine
EUDAMED SRN
FR-MF-000001182

Sources (1)

  • EUDAMED be2ea9a0-ec2f-4b7a-948e-926fb5d99a3b 61 fields · synced Jun 19, 2026