MD Atlas
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Data last updated: Apr 2025
KNEO FEMORAL TRIAL LEFT S01
++M483L091104F9
On Market
Class IIa
Regulation
EU MDR
Manufacturer
groupe lépine
Primary DI
+M483GKAEF3010
Reference
GKAEF301
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Identification
Primary DI
+M483GKAEF3010
Basic UDI-DI
++M483L091104F9
Reference
GKAEF301
Issuing Agency
—
ULID
T2HATNJ8
Classification
Risk Class
Class IIa
Regulation
EU MDR
Status
On Market
Device Types
Coming soon
Manufacturer
Manufacturer
groupe lépine
Manufacturer SRN
FR-MF-000001182
Manufacturer Status
Active
CND Nomenclature
V0599
CLINICAL PROCEDURES KITS NOT INCLUDED IN OTHER CLASSES - OTHER
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