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Data last updated: Apr 2025
MelanoRisk
B-03701126500081
On Market
Class I
Regulation
EU MDR
Manufacturer
PREDILIFE
Primary DI
03701126500081
Reference
MelanoRisk
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Identification
Primary DI
03701126500081
Basic UDI-DI
B-03701126500081
Reference
MelanoRisk
Issuing Agency
—
ULID
44CSV50Z
Classification
Risk Class
Class I
Regulation
EU MDR
Status
On Market
Device Types
Coming soon
Manufacturer
Manufacturer
PREDILIFE
Manufacturer SRN
FR-MF-000001863
Manufacturer Status
Active
CND Nomenclature
V0599
CLINICAL PROCEDURES KITS NOT INCLUDED IN OTHER CLASSES - OTHER
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