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RapidFor™ SARS-CoV-2 Rapid Antigen Test Kit (FIA)

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

Basic Information

Primary DI
08683347941049
Basic UDI-DI Code
B-08683347941049
Reference
VSCD03
Device Types
Single use
Regulation
Eu Ivdd
Classification
Eu Ivd General
Status
On The Market

Additional Description

This kit is used for in vitro qualitative detection of SARS-CoV-2 antigen. It is a lateral flow sandwich assay, intended for the qualitative detection of the nucleocapsid protein antigen from SARS-CoV-2 in nasopharyngeal (NP), nasal and oropharyngeal swab specimens directly.

CND Nomenclature Codes

Code Description
W0105040619 CORONAVIRUS [obsolete from 2025-01-01]
W0105099099 VIROLOGY - RT & POC - OTHER

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