Eu Ivdr Eu Ivd Class D On The Market 🇨🇳 China

SARS-CoV-2/FluA/FluB+ADV/RSV Antigen Combo Rapid Test Kit (LFIA)

Devices (same UDI-DI)
4
Certificates
1
Countries
12
Notified Bodies
1

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Basic Information

Primary DI
06974167891587
Basic UDI-DI Code
697416789100NQ
Reference
123143-01-102
Device Types
Single use New device Sterile
Regulation
Eu Ivdr
Classification
Eu Ivd Class D
Status
On The Market

Additional Description

SARS-CoV-2/FluA/FluB+ADV/RSV Antigen Combo Rapid Test Kit (LFIA) is an immunochromatography based one step in vitro test. It is designed for the qualitative detection of the SARS-CoV-2 virus, Influenza A virus, Influenza B virus, Adenovirus and Respiratory syncytial virus in human anterior nasal swab samples. The test results are used for the auxiliary diagnosis of respiratory pathogen infections, and are suitable for people with clinical symptoms such as fever, sore throat, cough, runny nose. The test kit is designed for use as self-testing. This test kit can be used independently by individuals who are 18 or older. For those under the age of 18, it should be operated or supervised by an adult. This test kit is not used in combination with other equipment and is not automated.

CND Nomenclature Codes

Code Description
W0105099099 VIROLOGY - RT & POC - OTHER

Certificates

Type Number
IVDR Technical Documentation EU-TDA-FI-06912-800035-2025-1

Available In Countries

🇧🇪 Belgium 🇩🇪 Germany 🇬🇷 Greece 🇪🇸 Spain 🇫🇮 Finland 🇫🇷 France 🇮🇹 Italy 🇳🇱 Netherlands 🇵🇱 Poland 🇵🇹 Portugal 🇷🇴 Romania 🇸🇪 Sweden

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