MD Atlas
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Data last updated: Apr 2025
FibroScan
3662264000000000000000368
On Market
Class IIa
Regulation
EU MDR
Manufacturer
Echosens
Primary DI
03662264001161
Reference
FibroScan 630
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Identification
Primary DI
03662264001161
Basic UDI-DI
3662264000000000000000368
Reference
FibroScan 630
Issuing Agency
—
ULID
RN39YX2V
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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