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Data last updated: Apr 2025
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36156NEOPROMK
On Market
Class I
Regulation
EU MDR
Manufacturer
GRAPHITE MEDICAL
Primary DI
03615650003584
Reference
NEO PRO 30 R
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Identification
Primary DI
03615650003584
Basic UDI-DI
36156NEOPROMK
Reference
NEO PRO 30 R
Issuing Agency
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ULID
9W12JYME
Classification
Risk Class
Class I
Regulation
EU MDR
Status
On Market
Device Types
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Manufacturer
Manufacturer
GRAPHITE MEDICAL
Manufacturer SRN
FR-MF-000002504
Manufacturer Status
Active
CND Nomenclature
V0599
CLINICAL PROCEDURES KITS NOT INCLUDED IN OTHER CLASSES - OTHER
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