Eu Ivdr Eu Ivd Class C On The Market ๐Ÿ‡ฉ๐Ÿ‡ช Germany

MYCOBACTERIA REAGENTS - OTHER

R-Biopharm AG ยท ๐Ÿ‡ฉ๐Ÿ‡ช Germany
Devices (same UDI-DI)
1
Certificates
0
Countries
32
Notified Bodies
0

Basic Information

Primary DI
04049095200069
Basic UDI-DI Code
4049095TN88020000UD
Reference
TN8802
Device Types
Single use
Regulation
Eu Ivdr
Classification
Eu Ivd Class C
Status
On The Market
Manufacturer
R-Biopharm AG

Additional Description

For in-vitro diagnostic use. The RIDAยฎQUICK TB is a manual immunochromatographic rapid test for the direct quantitative detection of interferon gamma induced protein 10 (IP-10) from human plasma samples of individuals with suspected Mycobacterium tuberculosis infection (including disease). This IVD test is intended for use in conjunction with the RIDAยฎTB Tubes for in-vitro stimulation with specific M. tuberculosis antigens. The RIDAยฎQUICK TB is a diagnostic aid for indirect detection of M. tuberculosis infection (including disease) and is intended for use in conjunction with risk assessments, radiographic examinations, and other clinical and laboratory findings. Negative results do not rule out M. tuberculosis infection and should not be used as the sole basis for diagnosis. The product is intended for professional use.

CND Nomenclature Codes

Code Description
W0105010799 MYCOBACTERIA REAGENTS - OTHER

Available In Countries

๐Ÿ‡ฆ๐Ÿ‡น Austria ๐Ÿ‡ง๐Ÿ‡ช Belgium ๐Ÿ‡ง๐Ÿ‡ฌ Bulgaria ๐Ÿ‡จ๐Ÿ‡พ Cyprus ๐Ÿ‡จ๐Ÿ‡ฟ Czechia ๐Ÿ‡ฉ๐Ÿ‡ช Germany ๐Ÿ‡ฉ๐Ÿ‡ฐ Denmark ๐Ÿ‡ช๐Ÿ‡ช Estonia ๐Ÿ‡ฌ๐Ÿ‡ท Greece ๐Ÿ‡ช๐Ÿ‡ธ Spain ๐Ÿ‡ซ๐Ÿ‡ฎ Finland ๐Ÿ‡ซ๐Ÿ‡ท France ๐Ÿ‡ญ๐Ÿ‡ท Croatia ๐Ÿ‡ญ๐Ÿ‡บ Hungary ๐Ÿ‡ฎ๐Ÿ‡ช Ireland ๐Ÿ‡ฎ๐Ÿ‡ธ Iceland ๐Ÿ‡ฎ๐Ÿ‡น Italy ๐Ÿ‡ฑ๐Ÿ‡ฎ Liechtenstein ๐Ÿ‡ฑ๐Ÿ‡น Lithuania ๐Ÿ‡ฑ๐Ÿ‡บ Luxembourg ๐Ÿ‡ฑ๐Ÿ‡ป Latvia ๐Ÿ‡ฒ๐Ÿ‡น Malta ๐Ÿ‡ณ๐Ÿ‡ฑ Netherlands ๐Ÿ‡ณ๐Ÿ‡ด Norway ๐Ÿ‡ต๐Ÿ‡ฑ Poland ๐Ÿ‡ต๐Ÿ‡น Portugal ๐Ÿ‡ท๐Ÿ‡ด Romania ๐Ÿ‡ธ๐Ÿ‡ช Sweden ๐Ÿ‡ธ๐Ÿ‡ฎ Slovenia ๐Ÿ‡ธ๐Ÿ‡ฐ Slovakia ๐Ÿ‡น๐Ÿ‡ท Tรผrkiye ๐Ÿ‡ฌ๐Ÿ‡ง United Kingdom

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