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Data last updated: Apr 2025
Newmedi
3760301945639Q
On Market
Class I
Regulation
EU MDR
Manufacturer
NEWMEDI
Primary DI
37603019456352
Reference
MIM563
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Identification
Primary DI
37603019456352
Basic UDI-DI
3760301945639Q
Reference
MIM563
Issuing Agency
—
ULID
FBEXA2XA
Classification
Risk Class
Class I
Regulation
EU MDR
Status
On Market
Device Types
Coming soon
Manufacturer
Manufacturer
NEWMEDI
Manufacturer SRN
FR-MF-000000922
Manufacturer Status
Active
CND Nomenclature
V0599
CLINICAL PROCEDURES KITS NOT INCLUDED IN OTHER CLASSES - OTHER
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Certificates
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Market Presence
Market presence
NL
DE
FR
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Countries on market
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