MD Atlas
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Data last updated: Apr 2025
DOUBLEFLO PATIENT TUBE SET
3661379FAB020002AEF
On Market
Class IIa
Regulation
EU MDR
Manufacturer
HEMODIA SAS
Primary DI
03661379223062
Reference
72205773
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Identification
Primary DI
03661379223062
Basic UDI-DI
3661379FAB020002AEF
Reference
72205773
Issuing Agency
—
ULID
MDWW9M09
Classification
Risk Class
Class IIa
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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Certificates
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