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Data last updated: Apr 2025
FibroScan
B-03662264001222
On Market
Class IIa
Regulation
EU MDR
Manufacturer
Echosens
Primary DI
03662264001222
Reference
FibroScan 230
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Identification
Primary DI
03662264001222
Basic UDI-DI
B-03662264001222
Reference
FibroScan 230
Issuing Agency
—
ULID
AA8HQ8GR
Classification
Risk Class
Class IIa
Regulation
EU MDR
Status
On Market
Device Types
Coming soon
Manufacturer
Manufacturer
Echosens
Manufacturer SRN
FR-MF-000003894
Manufacturer Status
Active
CND Nomenclature
V0599
CLINICAL PROCEDURES KITS NOT INCLUDED IN OTHER CLASSES - OTHER
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