Taiwan FDA registration 542046a9a1a9f1b83a27e15325e15452
ASK PREGNANCY ASSAY KIT
TW: “東耀” 懷孕檢測試劑組
Taiwan·Risk Class 2·MD·TONYAR BIOTECH. INC.·Registered Nov 16, 2016 – Nov 16, 2026ActiveRegistration details
- Analysis ID
- 542046a9a1a9f1b83a27e15325e15452
- License Form
- Ministry of Health Medical Device Manufacturing No. 005356
Company information
- Manufacturer
- TONYAR BIOTECH. INC.
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- TONYAR BIOTECH. INC.
Product details
- Intended Use
- Serum or urine is used to test whether serum or urine contains 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
Dates and status
- Registration Date
- Nov 16, 2016
- Expiry Date
- Nov 16, 2026
About this record
Access comprehensive regulatory information for ASK PREGNANCY ASSAY KIT in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 542046a9a1a9f1b83a27e15325e15452 and manufactured by TONYAR BIOTECH. INC.. The authorized representative in Taiwan is TONYAR BIOTECH. INC..
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