Taiwan FDA registration bae46ad396c0a1569777c925f28470a7
"Lifetech Corporation" Xiruixin atrial septal defect occluder
TW: “先健科技公司”希瑞心房間隔缺損封堵器
Taiwan·Risk Class 3·LIFETECH SCIENTIFIC (SHENZHEN) CO., LTD·Registered Apr 25, 2019 – Apr 25, 2029ActiveRegistration details
- Analysis ID
- bae46ad396c0a1569777c925f28470a7
- Customs Code
- DHA09200101106
Company information
- Manufacturer
- LIFETECH SCIENTIFIC (SHENZHEN) CO., LTD
- Manufacturer Country
- China
- Authorized Representative
- KAISEN MEDICAL CO., LTD
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- E Cardiovascular Medicine Science
- Product Type (Level 2)
- E.9999 Miscellaneous
- Import Information
- The use of this device shall comply with the provisions of the "Administrative Measures for the Implementation or Use of Medical Devices for Specific Medical Technology Inspection and Testing". Input;; Chinese goods
Dates and status
- Registration Date
- Apr 25, 2019
- Expiry Date
- Apr 25, 2029
About this record
Access comprehensive regulatory information for "Lifetech Corporation" Xiruixin atrial septal defect occluder in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number bae46ad396c0a1569777c925f28470a7 and manufactured by LIFETECH SCIENTIFIC (SHENZHEN) CO., LTD. The authorized representative in Taiwan is KAISEN MEDICAL CO., LTD.
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