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RapidFor™ Malaria P.f. / P.v. Rapid Test Kit

Devices (same UDI-DI)
1
Certificates
0
Countries
0
Notified Bodies
0

Basic Information

Primary DI
08683347941292
Basic UDI-DI Code
B-08683347941292
Reference
VMD22
Device Types
Single use
Regulation
Eu Ivdd
Classification
Eu Ivd General
Status
On The Market

Additional Description

This test kit is suitable for qualitative detection of Plasmodium falciparum and Plasmodium vivax in human venous whole blood in vitro and is suitable for auxiliary diagnosis of patients with suspected P. falciparum and P. vivax or examination of malaria cases.

CND Nomenclature Codes

Code Description
W0105090401 PLASMODIUM (MALARIA) - RT & POC

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