MD Atlas
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Data last updated: Apr 2025
FibroTest-ActiTest
B-03760373060137
On Market
Unknown
Regulation
EU MDR
Manufacturer
Biopredictive
Primary DI
03760373060137
Reference
FibroTest-ActiTest
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Identification
Primary DI
03760373060137
Basic UDI-DI
B-03760373060137
Reference
FibroTest-ActiTest
Issuing Agency
—
ULID
D58J7X92
Classification
Risk Class
Unknown
Regulation
EU MDR
Status
On Market
Device Types
Coming soon
Manufacturer
Manufacturer
Biopredictive
Manufacturer SRN
FR-MF-000003886
Manufacturer Status
Active
CND Nomenclature
V0599
CLINICAL PROCEDURES KITS NOT INCLUDED IN OTHER CLASSES - OTHER
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