MD Atlas
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Data last updated: Apr 2025
DRL
3666486OrthoKmyopieUQ
On Market
Class IIa
Regulation
EU MDR
Manufacturer
LABORATOIRE PRECILENS
Primary DI
03666486000810
Reference
DRL
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Identification
Primary DI
03666486000810
Basic UDI-DI
3666486OrthoKmyopieUQ
Reference
DRL
Issuing Agency
—
ULID
47TAZ5RA
Classification
Risk Class
Class IIa
Regulation
EU MDR
Status
On Market
Device Types
Coming soon
Manufacturer
Manufacturer
LABORATOIRE PRECILENS
Manufacturer SRN
FR-MF-000000913
Manufacturer Status
Active
CND Nomenclature
V0599
CLINICAL PROCEDURES KITS NOT INCLUDED IN OTHER CLASSES - OTHER
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