TECO RAPID PLASMA REAGIN (RPR) - Taiwan Registration a57f440690ac2083c7d9e4322aac63a7
Access comprehensive regulatory information for TECO RAPID PLASMA REAGIN (RPR) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number a57f440690ac2083c7d9e4322aac63a7 and manufactured by TECO DIAGNOSTICS. The authorized representative in Taiwan is HONEST MEDICAL INC..
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Device Details
Registration Details
a57f440690ac2083c7d9e4322aac63a7
Ministry of Health Medical Device Import No. 027713
DHA05602771301
Product Details
Non-treponemal qualitative and semi-quantitative rapid test reagent for the detection of reagin antibodies in human serum and plasma suffering from syphilis or other treponemal diseases.
C Immunology and microbiology devices
C3820 Treponemal pallidum non-treponemal reagent
Imported from abroad
Dates and Status
Oct 12, 2015
Oct 12, 2025