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RF Rapid Quantitative Test

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

Basic Information

Primary DI
06933260208043
Basic UDI-DI Code
B-06933260208043
Reference
BT0201001
Device Types
Single use
Regulation
Eu Ivdd
Classification
Eu Ivd General
Status
On The Market

Additional Description

The Biotime RF Rapid Quantitative Test is intended to quantify the concentration of RF in human serum, plasma and whole blood on Biotime FIA Analyzer by fluorescent immunoassay. The test is used as an aid detection of rheumatoid arthritis.

CND Nomenclature Codes

Code Description
W01021110 RHEUMATOID FACTORS

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