MD Atlas
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Data last updated: Apr 2025
CystoFlex™ F N
B-03760187912103
On Market
Class IIa
Regulation
EU MDR
Manufacturer
MAUNA KEA TECHNOLOGIES
Primary DI
03760187912103
Reference
FP-10038
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Identification
Primary DI
03760187912103
Basic UDI-DI
B-03760187912103
Reference
FP-10038
Issuing Agency
—
ULID
B2BQVK58
Classification
Risk Class
Class IIa
Regulation
EU MDR
Status
On Market
Device Types
Coming soon
Manufacturer
Manufacturer
MAUNA KEA TECHNOLOGIES
Manufacturer SRN
FR-MF-000000835
Manufacturer Status
Active
CND Nomenclature
V0599
CLINICAL PROCEDURES KITS NOT INCLUDED IN OTHER CLASSES - OTHER
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Certificates
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