MD Atlas
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Data last updated: Apr 2025
Cupule verte 250ml
3661379FAB0900001G6
On Market
Class I
Regulation
EU MDR
Manufacturer
HEMODIA SAS
Primary DI
03661379254172
Reference
104418
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Identification
Primary DI
03661379254172
Basic UDI-DI
3661379FAB0900001G6
Reference
104418
Issuing Agency
—
ULID
WD86T6DX
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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