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Data last updated: Apr 2025
BIOSYNEX AMPLIQUICK Lysis
353267F00061P82
On Market
IVDR Class A
Regulation
EU IVDR
Manufacturer
BIOSYNEX
Primary DI
03532678593074
Reference
3150059_SEC02
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Identification
Primary DI
03532678593074
Basic UDI-DI
353267F00061P82
Reference
3150059_SEC02
Issuing Agency
—
ULID
4V2GWTB3
Classification
Risk Class
IVDR Class A
Regulation
EU IVDR
Status
On Market
Device Types
Coming soon
Manufacturer
Manufacturer
BIOSYNEX
Manufacturer SRN
FR-MF-000014073
Manufacturer Status
Active
CND Nomenclature
V0599
CLINICAL PROCEDURES KITS NOT INCLUDED IN OTHER CLASSES - OTHER
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