Taiwan FDA registration 89fc9b7252c8e6b758d5d37f862fdffe
"Yida" Pylori Reagent (Unsterilized)
TW: "醫達" 幽門桿菌試劑 (未滅菌)
Taiwan·Risk Class 1·MD BIOTECH CORPORATION·Registered Nov 01, 2012 – Nov 01, 2017CancelledRegistration details
- Analysis ID
- 89fc9b7252c8e6b758d5d37f862fdffe
- Customs Code
- DHA04401232804
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
- Nov 01, 2012
- Expiry Date
- Nov 01, 2017
- Cancellation Date
- Aug 01, 2019
Cancellation information
- Status
- Logged out
- Reason
- 未展延而逾期者;;自請註銷
About this record
Access comprehensive regulatory information for "Yida" 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 89fc9b7252c8e6b758d5d37f862fdffe and manufactured by MD BIOTECH CORPORATION. The authorized representative in Taiwan is E-TAKE TECHNOLOGY CO., LTD..
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