Taiwan FDA registration 06246aefe85f1430270b4d1253038f15
"Lifetech Technologies" Sieker lumen capture system
TW: “先健科技公司” 西克爾管腔抓捕系統
Taiwan·Risk Class 2·LIFETECH SCIENTIFIC (SHENZHEN) CO., LTD·Registered Sep 17, 2018 – Sep 17, 2028ActiveRegistration details
- Analysis ID
- 06246aefe85f1430270b4d1253038f15
- Customs Code
- DHA09200092904
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.1250 Percutaneous catheters
- Import Information
- Input;; Chinese goods
Dates and status
- Registration Date
- Sep 17, 2018
- Expiry Date
- Sep 17, 2028
About this record
Access comprehensive regulatory information for "Lifetech Technologies" Sieker lumen capture system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 06246aefe85f1430270b4d1253038f15 and manufactured by LIFETECH SCIENTIFIC (SHENZHEN) CO., LTD. The authorized representative in Taiwan is KAISEN MEDICAL CO., LTD.
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