MD Atlas
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Data last updated: Apr 2025
K Myo
3770011995KMyo95
On Market
Class I
Regulation
EU MDR
Manufacturer
KINVENT Biomecanique
Primary DI
03770011995707
Reference
MP.10.02.FN
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Identification
Primary DI
03770011995707
Basic UDI-DI
3770011995KMyo95
Reference
MP.10.02.FN
Issuing Agency
—
ULID
VB48KY3T
Classification
Risk Class
Class I
Regulation
EU MDR
Status
On Market
Device Types
Coming soon
Manufacturer
Manufacturer
KINVENT Biomecanique
Manufacturer SRN
FR-MF-000031884
Manufacturer Status
Active
CND Nomenclature
V0599
CLINICAL PROCEDURES KITS NOT INCLUDED IN OTHER CLASSES - OTHER
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