Eu Ivdd Eu Ivd General On The Market 🇨🇳 China

VIROLOGY - RT & POC - OTHER

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

Basic Information

Primary DI
06970664751393
Basic UDI-DI Code
B-06970664751393
Reference
50Tests/Kit
Device Types
None provided
Regulation
Eu Ivdd
Classification
Eu Ivd General
Status
On The Market

Additional Description

COVID-19 Nucleic Acid Test Kit(fluorescence PCR)is an in vitro diagnostic real-time reverse transcription-PCR assay for the qualitative detection of SARS-CoV-2 nucleic acidsin throat (oropharyngeal) swabs, nasopharyngeal swabs, anterior nasal swabs, mid-turbinatenasal swabs, nasal washes, nasal aspirates and bronchoalveolar lavage fluid (BALF) fromindividuals who are suspected of COVID-19 by their healthcare provider.

CND Nomenclature Codes

Code Description
W0105099099 VIROLOGY - RT & POC - OTHER

Similar Devices

Other on-the-market devices with the same classification (Eu Ivd General) and regulation (EU IVDD).

View all