Taiwan FDA registration 8d0493b6c05b4fefef42750e433e47d3
"Safety Assessment" Pylori Antibody Rapid Test Reagent (Unsterilized)
TW: "安評" 幽門桿菌抗體快速檢驗試劑 (未滅菌)
Taiwan·Risk Class 1·MP BIOMEDICALS ASIA PACIFIC PTE. LTD.·Registered Dec 18, 2012 – Dec 18, 2017CancelledRegistration details
- Analysis ID
- 8d0493b6c05b4fefef42750e433e47d3
- Customs Code
- DHA04401249905
Company information
- Manufacturer
- MP BIOMEDICALS ASIA PACIFIC PTE. LTD.
- Manufacturer Country
- Singapore
- Authorized Representative
- JOLEX INTERNATIONAL CO., LTD.
Product details
- Intended Use
- Limited to the first level identification range of the Measures for the Administration of Medical Devices "Helicobacter Serological 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
- import
Dates and status
- Registration Date
- Dec 18, 2012
- Expiry Date
- Dec 18, 2017
- Cancellation Date
- Jan 17, 2019
Cancellation information
- Status
- Logged out
- Reason
- 自請註銷
About this record
Access comprehensive regulatory information for "Safety Assessment" Pylori Antibody Rapid Test 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 8d0493b6c05b4fefef42750e433e47d3 and manufactured by MP BIOMEDICALS ASIA PACIFIC PTE. LTD.. The authorized representative in Taiwan is JOLEX INTERNATIONAL CO., LTD..
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