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Data last updated: Apr 2025
WiTOF (branded Idmed)
3665023WiTOF-MUR2
On Market
Class IIa
Regulation
EU MDR
Manufacturer
Idmed
Primary DI
03665023000535
Reference
WiTOF-MU
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Identification
Primary DI
03665023000535
Basic UDI-DI
3665023WiTOF-MUR2
Reference
WiTOF-MU
Issuing Agency
—
ULID
EAZQA203
Classification
Risk Class
Class IIa
Regulation
EU MDR
Status
On Market
Device Types
Coming soon
Manufacturer
Manufacturer
Idmed
Manufacturer SRN
FR-MF-000002402
Manufacturer Status
Active
CND Nomenclature
V0599
CLINICAL PROCEDURES KITS NOT INCLUDED IN OTHER CLASSES - OTHER
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