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Flexion Hemi Spacer H11

EUDAMED

Class I (EU MDR)

Ref GNA BO011Model Class Ir InstrumentRef GNANW175

by groupe lépine

Identity

Trade Name
FLEXION HEMI SPACER H11 EUDAMED
Device Name
Class Ir Instrument EUDAMED
Model / Reference
Class Ir Instrument EUDAMED
GNA BO011 EUDAMED
GNANW175 EUDAMED

Identifiers

Primary DI / UDI-DI
+M483GNABO0110 EUDAMED
+M483GNANW1750 EUDAMED
Basic UDI-DI
++M483L0909Z3 EUDAMED
Direct Marketing DI
+M483GNABO0110 EUDAMED
+M483GNANW1750 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

Flexion Hemi Spacer H11 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 (2)

  • EUDAMED 1e703351-dca7-4dcc-9466-1067ee171bde 61 fields · synced Jul 9, 2026
  • EUDAMED f24c05dc-ca45-46c0-bc76-ff8faf4fe72e 61 fields · synced May 17, 2026