MD Atlas
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Data last updated: Apr 2025
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B-37603610302270
On Market
Class I
Regulation
EU MDR
Manufacturer
SÊMEIA
Primary DI
37603610302270
Reference
RhumatoWise
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Identification
Primary DI
37603610302270
Basic UDI-DI
B-37603610302270
Reference
RhumatoWise
Issuing Agency
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ULID
Q4381BBB
Classification
Risk Class
Class I
Regulation
EU MDR
Status
On Market
Device Types
Coming soon
Manufacturer
Manufacturer
SÊMEIA
Manufacturer SRN
FR-MF-000018486
Manufacturer Status
Active
CND Nomenclature
V0599
CLINICAL PROCEDURES KITS NOT INCLUDED IN OTHER CLASSES - OTHER
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FR
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