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Data last updated: Apr 2025
WiTOF
3665023WiTOF-SystemNZ
On Market
Class IIa
Regulation
EU MDR
Manufacturer
Idmed
Primary DI
03665023000610
Reference
WiTOF-DEMO
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Identification
Primary DI
03665023000610
Basic UDI-DI
3665023WiTOF-SystemNZ
Reference
WiTOF-DEMO
Issuing Agency
—
ULID
KWG806K7
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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