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Data last updated: Apr 2025
Liflow® 3.0
37007197LiflowAQ
On Market
Class IIa
Regulation
EU MDR
Manufacturer
INTRASENSE
Primary DI
03700719701096
Reference
Liflow® 3.0
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Identification
Primary DI
03700719701096
Basic UDI-DI
37007197LiflowAQ
Reference
Liflow® 3.0
Issuing Agency
—
ULID
2ERQ41S2
Classification
Risk Class
Class IIa
Regulation
EU MDR
Status
On Market
Device Types
Coming soon
Manufacturer
Manufacturer
INTRASENSE
Manufacturer SRN
FR-MF-000001551
Manufacturer Status
Active
CND Nomenclature
V0599
CLINICAL PROCEDURES KITS NOT INCLUDED IN OTHER CLASSES - OTHER
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