Taiwan FDA registration dd4600337ed668552777ddb636aa8064
"Shinto" pregnancy test double test - serum/urine
TW: “信東”孕準懷孕試劑雙測試-血清/尿液
Taiwan·Risk Class 2·TONYAR BIOTECH. INC.·Registered Jul 06, 2012 – Sep 28, 2020CancelledRegistration details
- Analysis ID
- dd4600337ed668552777ddb636aa8064
Company information
- Manufacturer
- TONYAR BIOTECH. INC.
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- TAIWAN BIOTECH CO., LTD.
Product details
- Intended Use
- 利用定性法進行血清或尿液中是否含有人類絨毛膜刺激生殖激素(HCG, human chorionic gonadotropin)之測試.
- Product Type (Level 1)
- A Clinical chemistry and clinical toxicology
- Product Type (Level 2)
- A.1155 Human chorionic gonadotropin testing system
- Import Information
- Domestic;; Contract manufacturing
Dates and status
- Registration Date
- Jul 06, 2012
- Expiry Date
- Sep 28, 2020
- Cancellation Date
- Jan 03, 2018
Cancellation information
- Status
- Logged out
- Reason
- 自請註銷
About this record
Access comprehensive regulatory information for "Shinto" pregnancy test double test - serum/urine in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number dd4600337ed668552777ddb636aa8064 and manufactured by TONYAR BIOTECH. INC.. The authorized representative in Taiwan is TAIWAN BIOTECH CO., LTD..
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