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Kneo Keel Punch S01-S06

EUDAMED

Class I (EU MDR)

Ref GKACT001Model Class Ir Instrument

by groupe lépine

Identity

Trade Name
KNEO KEEL PUNCH S01-S06 EUDAMED
Device Name
Class Ir Instrument EUDAMED
Model / Reference
Class Ir Instrument EUDAMED
GKACT001 EUDAMED

Identifiers

Primary DI / UDI-DI
+M483GKACT0010 EUDAMED
Basic UDI-DI
++M483L0909Z3 EUDAMED
Direct Marketing DI
+M483GKACT0010 EUDAMED
EMDN Code
L090999 ORTHOPAEDIC SURGERY CUTTING 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

Category: Bone cutting forceps, reusable

Kneo Keel Punch S01-S06 by groupe lépine — Class I — MDR — listed in EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Bone cutting forceps, reusable.

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 c05f8a4e-f675-4438-b10e-fb4544fd95ee 61 fields · synced Jun 18, 2026