MD Atlas
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Data last updated: Apr 2025
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37015381CLASSIC-CERMETZF
On Market
Class I
Regulation
EU MDR
Manufacturer
OCTIKA
Primary DI
03700846257572
Reference
P238_C1
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Identification
Primary DI
03700846257572
Basic UDI-DI
37015381CLASSIC-CERMETZF
Reference
P238_C1
Issuing Agency
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ULID
G230RRFZ
Classification
Risk Class
Class I
Regulation
EU MDR
Status
On Market
Device Types
Coming soon
Manufacturer
Manufacturer
OCTIKA
Manufacturer SRN
FR-MF-000050179
Manufacturer Status
Active
CND Nomenclature
V0599
CLINICAL PROCEDURES KITS NOT INCLUDED IN OTHER CLASSES - OTHER
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