Taiwan FDA registration 7bdbc696e46bfa78005a6fa2715643a7
"Lifetech Technologies" Hertel ventricular septal defect occluder
TW: “先健科技公司”赫特爾心室間隔缺損封堵器
Taiwan·Risk Class 3·LIFETECH SCIENTIFIC (SHENZHEN) CO., LTD·Registered Aug 20, 2015 – Aug 20, 2025ExpiredRegistration details
- Analysis ID
- 7bdbc696e46bfa78005a6fa2715643a7
- Customs Code
- DHA09200070304
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
- Input;; Chinese goods
Dates and status
- Registration Date
- Aug 20, 2015
- Expiry Date
- Aug 20, 2025
About this record
Access comprehensive regulatory information for "Lifetech Technologies" Hertel 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 7bdbc696e46bfa78005a6fa2715643a7 and manufactured by LIFETECH SCIENTIFIC (SHENZHEN) CO., LTD. The authorized representative in Taiwan is KAISEN MEDICAL CO., LTD.
This page provides complete technical specifications, regulatory compliance details. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.
Free DatabasePowered by Pure Global AI89,000+ Devices