MD Atlas
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Data last updated: Apr 2025
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37601BATFW
On Market
Class I
Regulation
EU MDR
Manufacturer
Inter.med
Primary DI
03760139501935
Reference
C103
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Identification
Primary DI
03760139501935
Basic UDI-DI
37601BATFW
Reference
C103
Issuing Agency
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ULID
1GQE945V
Classification
Risk Class
Class I
Regulation
EU MDR
Status
On Market
Device Types
Coming soon
Manufacturer
Manufacturer
Inter.med
Manufacturer SRN
FR-MF-000000461
Manufacturer Status
Active
CND Nomenclature
V0599
CLINICAL PROCEDURES KITS NOT INCLUDED IN OTHER CLASSES - OTHER
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