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Data last updated: Apr 2025
Spatule de réintervention LASIK Fox
37004836Spatulas1NJ
On Market
Class I
Regulation
EU MDR
Manufacturer
Moria S.A.
Primary DI
03700483605675
Reference
19080
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Identification
Primary DI
03700483605675
Basic UDI-DI
37004836Spatulas1NJ
Reference
19080
Issuing Agency
—
ULID
384Y9GBZ
Classification
Risk Class
Class I
Regulation
EU MDR
Status
On Market
Device Types
Coming soon
Manufacturer
Manufacturer
Moria S.A.
Manufacturer SRN
FR-MF-000000336
Manufacturer Status
Active
CND Nomenclature
V0599
CLINICAL PROCEDURES KITS NOT INCLUDED IN OTHER CLASSES - OTHER
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DE
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IT
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