Eu Ivdd
Eu Ivd General
On The Market
🇨🇳 China
SARS‐CoV‐2 Antigen Rapid Test Kit
Devices (same UDI-DI)
1
Certificates
0
Countries
7
Notified Bodies
0
Basic Information
- Primary DI
- 16974169670101
- Basic UDI-DI Code
- B-16974169670101
- Reference
- 1 set
- Device Types
-
Single use
- Regulation
- Eu Ivdd
- Classification
- Eu Ivd General
- Status
- On The Market
- Manufacturer
- Shenzhen Lvshiyuan Biotechnology Co., Ltd.
Additional Description
The Green Spring® SARS‐CoV‐2 Antigen Rapid Test is designed for the rapid qualitative detection of SARS‐CoV‐2 nucleocapsid protein antigen in human saliva, nasal, nasopharyngeal, or oropharyngeal swab specimens. The results are used to detect SARS‐CoV‐ 2 antigens.
CND Nomenclature Codes
| Code | Description |
|---|---|
| W0102019099 | SPECIFIC PROTEINS - OTHER |
Available In Countries
🇧🇪 Belgium
🇩🇪 Germany
🇪🇸 Spain
🇫🇷 France
🇭🇷 Croatia
🇮🇹 Italy
🇸🇪 Sweden
Similar Devices
Other on-the-market devices with the same classification (Eu Ivd General) and regulation (EU IVDD).
BluBox
Device
EU IVDD
·
Eu Ivd General
·Blusense Diagnostics ApS·On the market·5 countries
extendSURE™ HbA1c Liquid Controls
Device
EU IVDD
·
Eu Ivd General
·Canterbury Scientific Limited·On the market·19 countries
ViroTrack Sero COVID-19 Total Ab
Device
EU IVDD
·
Eu Ivd General
·Blusense Diagnostics ApS·On the market·5 countries
extendSURETM Haemoglobin F and A2 Calibrators
Device
EU IVDD
·
Eu Ivd General
·Canterbury Scientific Limited·On the market·8 countries
extendSURE™ Haemoglobin F and A2 Controls
Device
EU IVDD
·
Eu Ivd General
·Canterbury Scientific Limited·On the market·8 countries
extendSURE™ HbA1c Liquid Controls
Device
EU IVDD
·
Eu Ivd General
·Canterbury Scientific Limited·On the market·19 countries