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Data last updated: Apr 2025
Evidence EEG61
376037501NM-G091.00QW
On Market
Class IIa
Regulation
EU MDR
Manufacturer
NEUROMED
Primary DI
03760375010079
Reference
212002-02-NMD
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Identification
Primary DI
03760375010079
Basic UDI-DI
376037501NM-G091.00QW
Reference
212002-02-NMD
Issuing Agency
—
ULID
E1DTK9V0
Classification
Risk Class
Class IIa
Regulation
EU MDR
Status
On Market
Device Types
Coming soon
Manufacturer
Manufacturer
NEUROMED
Manufacturer SRN
FR-MF-000028522
Manufacturer Status
Active
CND Nomenclature
V0599
CLINICAL PROCEDURES KITS NOT INCLUDED IN OTHER CLASSES - OTHER
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