MD Atlas
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Data last updated: Apr 2025
FibroScan
366226400000000000000076G
On Market
Class IIa
Regulation
EU MDR
Manufacturer
Echosens
Primary DI
03662264001208
Reference
FibroScan 430
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Identification
Primary DI
03662264001208
Basic UDI-DI
366226400000000000000076G
Reference
FibroScan 430
Issuing Agency
—
ULID
H0EX87XZ
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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