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Data last updated: Apr 2025
NEOFOOT G40
3770033655NEOFOO2023NFJW
On Market
Class I
Regulation
EU MDR
Manufacturer
NEOORTHOPEDIE
Primary DI
03770033655061
Reference
NEO2023NFG40
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Identification
Primary DI
03770033655061
Basic UDI-DI
3770033655NEOFOO2023NFJW
Reference
NEO2023NFG40
Issuing Agency
—
ULID
SC7FXXWG
Classification
Risk Class
Class I
Regulation
EU MDR
Status
On Market
Device Types
Coming soon
Manufacturer
Manufacturer
NEOORTHOPEDIE
Manufacturer SRN
FR-MF-000038032
Manufacturer Status
Active
CND Nomenclature
V0599
CLINICAL PROCEDURES KITS NOT INCLUDED IN OTHER CLASSES - OTHER
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