Taiwan FDA registration 097197bb8fec3feffab539fd59342d33
"E-TAKE" HP-UT&T (Non-Sterile)
TW: "醫達" 幽門桿菌試劑 (未滅菌)
Taiwan·Risk Class 1·MD·MD BIOTECH CORPORATION·Registered Apr 19, 2016 – Apr 19, 2021CancelledRegistration details
- Analysis ID
- 097197bb8fec3feffab539fd59342d33
- License Form
- Ministry of Health Medical Device Import No. 016417
- Customs Code
- DHA09401641703
Company information
- Manufacturer
- MD BIOTECH CORPORATION
- Manufacturer Country
- United States
- Authorized Representative
- E-TAKE TECHNOLOGY CO., LTD.
Product details
- Product Type (Level 1)
- C Immunology and microbiology devices
- Product Type (Level 2)
- C0003 Helicobacter serological reagent
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Apr 19, 2016
- Expiry Date
- Apr 19, 2021
- Cancellation Date
- Jun 22, 2022
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "E-TAKE" HP-UT&T (Non-Sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 097197bb8fec3feffab539fd59342d33 and manufactured by MD BIOTECH CORPORATION. The authorized representative in Taiwan is E-TAKE TECHNOLOGY CO., LTD..
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