Taiwan FDA registration 82bc7d5ffe097e89e97a68e8041a2a20
"Lifetech Corporation" Hertel atrial septal defect occluder
TW: “先健科技公司”赫特爾心房間隔缺損封堵器
Taiwan·Risk Class 3·LIFETECH SCIENTIFIC (SHENZHEN) CO., LTD·Registered Aug 20, 2015 – Aug 20, 2025ExpiredRegistration details
- Analysis ID
- 82bc7d5ffe097e89e97a68e8041a2a20
- Customs Code
- DHA09200070100
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
- Import Information
- Chinese goods;; input
Dates and status
- Registration Date
- Aug 20, 2015
- Expiry Date
- Aug 20, 2025
About this record
Access comprehensive regulatory information for "Lifetech Corporation" Hertel 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 82bc7d5ffe097e89e97a68e8041a2a20 and manufactured by LIFETECH SCIENTIFIC (SHENZHEN) CO., LTD. The authorized representative in Taiwan is KAISEN MEDICAL CO., LTD.
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