Taiwan FDA registration 9974fb7fd804d7fc6a28d929ba95c4ba
"Gretel" Pylori reagent (unsterilized)
TW: "格雷特" 幽門桿菌試劑 (未滅菌)
Taiwan·Risk Class 1·TONYAR BIOTECH. INC.·Registered Aug 31, 2017 – Aug 31, 2027ActiveRegistration details
- Analysis ID
- 9974fb7fd804d7fc6a28d929ba95c4ba
Company information
- Manufacturer
- TONYAR BIOTECH. INC.
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- GREAT BIOTECH LIMITED
Product details
- Intended Use
- Limited to the classification and grading management of medical devices, the first level identification range of "Helicobacter serum reagent (C.0003)".
- Product Type (Level 1)
- C Immunology and microbiology
- Product Type (Level 2)
- C.0003 螺旋桿菌屬血清試劑
- Import Information
- Domestic;; Contract manufacturing
Dates and status
- Registration Date
- Aug 31, 2017
- Expiry Date
- Aug 31, 2027
About this record
Access comprehensive regulatory information for "Gretel" Pylori reagent (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 9974fb7fd804d7fc6a28d929ba95c4ba and manufactured by TONYAR BIOTECH. INC.. The authorized representative in Taiwan is GREAT BIOTECH LIMITED.
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