MD Atlas
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Data last updated: Apr 2025
fauteuil de consultation NIDEK
37008623FAU0015Y
On Market
Class I
Regulation
EU MDR
Manufacturer
NIDEK SA
Primary DI
03700862300207
Reference
HFE0001
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Identification
Primary DI
03700862300207
Basic UDI-DI
37008623FAU0015Y
Reference
HFE0001
Issuing Agency
—
ULID
KQVRF6XR
Classification
Risk Class
Class I
Regulation
EU MDR
Status
On Market
Device Types
Coming soon
Manufacturer
Manufacturer
NIDEK SA
Manufacturer SRN
FR-MF-000000493
Manufacturer Status
Active
CND Nomenclature
V0599
CLINICAL PROCEDURES KITS NOT INCLUDED IN OTHER CLASSES - OTHER
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Certificates
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