MD Atlas
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Data last updated: Apr 2025
GastroFlex™ N
376018791NCM2DX
On Market
Class IIa
Regulation
EU MDR
Manufacturer
MAUNA KEA TECHNOLOGIES
Primary DI
03760187912028
Reference
FP-10030
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Identification
Primary DI
03760187912028
Basic UDI-DI
376018791NCM2DX
Reference
FP-10030
Issuing Agency
—
ULID
7SNEC4VW
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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