MD Atlas
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Data last updated: Apr 2025
Cupule 120ml verte
3661379FAB0900001G6
On Market
Class I
Regulation
EU MDR
Manufacturer
HEMODIA SAS
Primary DI
03661379235935
Reference
104241
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Identification
Primary DI
03661379235935
Basic UDI-DI
3661379FAB0900001G6
Reference
104241
Issuing Agency
—
ULID
9SESKDES
Classification
Risk Class
Class I
Regulation
EU MDR
Status
On Market
Device Types
Coming soon
Manufacturer
Manufacturer
HEMODIA SAS
Manufacturer SRN
FR-MF-000007191
Manufacturer Status
Active
CND Nomenclature
V0599
CLINICAL PROCEDURES KITS NOT INCLUDED IN OTHER CLASSES - OTHER
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