MD Atlas
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Data last updated: Apr 2025
TUBULURE RENFORCEE
B-03661379120781
On Market
Class IIa
Regulation
EU MDR
Manufacturer
HEMODIA SAS
Primary DI
03661379120781
Reference
5123_B
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Identification
Primary DI
03661379120781
Basic UDI-DI
B-03661379120781
Reference
5123_B
Issuing Agency
—
ULID
02VG12WH
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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