Taiwan FDA registration 210899f7dbc6cfbf1c35da9dec1b14dd
"Lifetech Corporation" Xirui elastic heart atrial septal defect occluder
TW: “先健科技公司”希瑞彈性心房間隔缺損封堵器
Taiwan·Risk Class 3·LIFETECH SCIENTIFIC (SHENZHEN) CO., LTD·Registered Jul 12, 2019 – Jul 12, 2024ExpiredRegistration details
- Analysis ID
- 210899f7dbc6cfbf1c35da9dec1b14dd
- Customs Code
- DHA09200102708
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
- Chinese goods;; input
Dates and status
- Registration Date
- Jul 12, 2019
- Expiry Date
- Jul 12, 2024
About this record
Access comprehensive regulatory information for "Lifetech Corporation" Xirui elastic heart 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 210899f7dbc6cfbf1c35da9dec1b14dd and manufactured by LIFETECH SCIENTIFIC (SHENZHEN) CO., LTD. The authorized representative in Taiwan is KAISEN MEDICAL CO., LTD.
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