Taiwan FDA registration a57f440690ac2083c7d9e4322aac63a7
TECO RAPID PLASMA REAGIN (RPR)
TW: 鐵可 快速血漿反應素試劑組
Taiwan·Risk Class 2·MD·TECO DIAGNOSTICS·Registered Oct 12, 2015 – Oct 12, 2025ExpiredRegistration details
- Analysis ID
- a57f440690ac2083c7d9e4322aac63a7
- License Form
- Ministry of Health Medical Device Import No. 027713
- Customs Code
- DHA05602771301
Company information
- Manufacturer
- TECO DIAGNOSTICS
- Manufacturer Country
- United States
- Authorized Representative
- HONEST MEDICAL INC.
Product details
- Intended Use
- 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.
- Product Type (Level 1)
- C Immunology and microbiology devices
- Product Type (Level 2)
- C3820 Treponemal pallidum non-treponemal reagent
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Oct 12, 2015
- Expiry Date
- Oct 12, 2025
About this record
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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