Taiwan FDA registration 5d1a86c37c36c9b03a3844e1d00a9082
"Lifetech Corporation" Ciri ventricular septal defect occluder
TW: “先健科技公司”希瑞心室間隔缺損封堵器
Taiwan·Risk Class 3·LIFETECH SCIENTIFIC (SHENZHEN) CO., LTD·Registered Jul 12, 2019 – Jul 12, 2029ActiveRegistration details
- Analysis ID
- 5d1a86c37c36c9b03a3844e1d00a9082
- Customs Code
- DHA09200102800
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, 2029
About this record
Access comprehensive regulatory information for "Lifetech Corporation" Ciri ventricular 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 5d1a86c37c36c9b03a3844e1d00a9082 and manufactured by LIFETECH SCIENTIFIC (SHENZHEN) CO., LTD. The authorized representative in Taiwan is KAISEN MEDICAL CO., LTD.
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