MD Atlas
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Data last updated: Apr 2025
Porte Tablette
376039415030BX
On Market
Class I
Regulation
EU MDR
Manufacturer
OBRO
Primary DI
03760394150220
Reference
CS321
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Identification
Primary DI
03760394150220
Basic UDI-DI
376039415030BX
Reference
CS321
Issuing Agency
—
ULID
H7K5C9RZ
Classification
Risk Class
Class I
Regulation
EU MDR
Status
On Market
Device Types
Coming soon
Manufacturer
Manufacturer
OBRO
Manufacturer SRN
FR-MF-000019841
Manufacturer Status
Active
CND Nomenclature
V0599
CLINICAL PROCEDURES KITS NOT INCLUDED IN OTHER CLASSES - OTHER
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