Taiwan FDA registration c69f59e0f56b73e5c44658d0fc4bf8a5
"Yida" pylori antigen test reagent (unsterilized)
TW: “醫達”幽門桿菌抗原檢驗試劑(未滅菌)
Taiwan·Risk Class 1·MD BIOTECH CORPORATION·Registered Jan 25, 2013 – Jan 25, 2018CancelledRegistration details
- Analysis ID
- c69f59e0f56b73e5c44658d0fc4bf8a5
- Customs Code
- DHA04401264108
Company information
- Manufacturer
- MD BIOTECH CORPORATION
- Manufacturer Country
- United States
- Authorized Representative
- E-TAKE TECHNOLOGY 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
- Jan 25, 2013
- Expiry Date
- Jan 25, 2018
- Cancellation Date
- Jul 30, 2019
Cancellation information
- Status
- Logged out
- Reason
- 自請註銷
About this record
Access comprehensive regulatory information for "Yida" pylori antigen 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 c69f59e0f56b73e5c44658d0fc4bf8a5 and manufactured by MD BIOTECH CORPORATION. The authorized representative in Taiwan is E-TAKE TECHNOLOGY CO., LTD..
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