MD Atlas
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Data last updated: Apr 2025
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3666663GOBELET35
On Market
Class I
Regulation
EU MDR
Manufacturer
Rovipharm
Primary DI
03760337568136
Reference
26105031
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Identification
Primary DI
03760337568136
Basic UDI-DI
3666663GOBELET35
Reference
26105031
Issuing Agency
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ULID
KTH9NPHA
Classification
Risk Class
Class I
Regulation
EU MDR
Status
On Market
Device Types
Coming soon
Manufacturer
Manufacturer
Rovipharm
Manufacturer SRN
FR-MF-000000673
Manufacturer Status
Active
CND Nomenclature
V0599
CLINICAL PROCEDURES KITS NOT INCLUDED IN OTHER CLASSES - OTHER
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