MD Atlas
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Data last updated: Apr 2025
—
37009775porte-implant8K
On Market
Class I
Regulation
EU MDR
Manufacturer
EUROTEKNIKA
Primary DI
03700977507089
Reference
CGC_PI_3N
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Identification
Primary DI
03700977507089
Basic UDI-DI
37009775porte-implant8K
Reference
CGC_PI_3N
Issuing Agency
—
ULID
EG5G0SRD
Classification
Risk Class
Class I
Regulation
EU MDR
Status
On Market
Device Types
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Manufacturer
Manufacturer
EUROTEKNIKA
Manufacturer SRN
FR-MF-000004032
Manufacturer Status
Active
CND Nomenclature
V0599
CLINICAL PROCEDURES KITS NOT INCLUDED IN OTHER CLASSES - OTHER
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