Taiwan FDA registration bafc3f8970b47834d882d3a668f4a0dc
LOVECARE HCG RAPID TEST
TW: 婕朵快速驗孕試劑系統
Taiwan·Risk Class 2·MD·TONYAR BIOTECH. INC.·Registered Jan 18, 2012 – Sep 28, 2025ExpiredRegistration details
- Analysis ID
- bafc3f8970b47834d882d3a668f4a0dc
- License Form
- Department of Health Medical Device Manufacturing No. 003508
- Customs Code
- DHY00500350807
Company information
- Manufacturer
- TONYAR BIOTECH. INC.
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- JIEDUO ENTERPRISE CO., LTD.
Product details
- Intended Use
- The change in efficacy (removal of serum source and addition of non-specialist use) is the qualitative test of urine for human chorionic gonadotropin (HCG).
- Product Type (Level 1)
- A Clinical chemistry and clinical toxicology
- Product Type (Level 2)
- A1155 Human chorionic gonadotropin test system
- Import Information
- Produced in Taiwan, China; Contract manufacturing
Dates and status
- Registration Date
- Jan 18, 2012
- Expiry Date
- Sep 28, 2025
About this record
Access comprehensive regulatory information for LOVECARE HCG RAPID TEST in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number bafc3f8970b47834d882d3a668f4a0dc and manufactured by TONYAR BIOTECH. INC.. The authorized representative in Taiwan is JIEDUO ENTERPRISE CO., LTD..
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