MD Atlas
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Data last updated: Apr 2025
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3770013995LF0000SD
On Market
Class IIa
Regulation
EU MDR
Manufacturer
i-SEP
Primary DI
33770013995683
Reference
LF0000M1
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Identification
Primary DI
33770013995683
Basic UDI-DI
3770013995LF0000SD
Reference
LF0000M1
Issuing Agency
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ULID
REHWZRAX
Classification
Risk Class
Class IIa
Regulation
EU MDR
Status
On Market
Device Types
Coming soon
Manufacturer
Manufacturer
i-SEP
Manufacturer SRN
FR-MF-000000363
Manufacturer Status
Active
CND Nomenclature
V0599
CLINICAL PROCEDURES KITS NOT INCLUDED IN OTHER CLASSES - OTHER
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