MD Atlas
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Data last updated: Apr 2025
OSLO T39
332254057L3
On Market
Class I
Regulation
EU MDR
Manufacturer
GIBAUD
Primary DI
03322541072368
Reference
8388-39
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Identification
Primary DI
03322541072368
Basic UDI-DI
332254057L3
Reference
8388-39
Issuing Agency
—
ULID
9EYA5NRX
Classification
Risk Class
Class I
Regulation
EU MDR
Status
On Market
Device Types
Coming soon
Manufacturer
Manufacturer
GIBAUD
Manufacturer SRN
FR-MF-000014279
Manufacturer Status
Active
CND Nomenclature
V0599
CLINICAL PROCEDURES KITS NOT INCLUDED IN OTHER CLASSES - OTHER
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