MD Atlas
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Data last updated: Apr 2025
ASPIROTUB®
37601TUBKG
On Market
Class IIa
Regulation
EU MDR
Manufacturer
Inter.med
Primary DI
03760139502598
Reference
C347S, C347, C345, C345S
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Identification
Primary DI
03760139502598
Basic UDI-DI
37601TUBKG
Reference
C347S, C347, C345, C345S
Issuing Agency
—
ULID
MNFEQ53J
Classification
Risk Class
Class IIa
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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