Taiwan FDA registration d0dae6312c133c01ad3dd5c5c0e144e7
“Lifetech Scientific” LAmbre Left Atrial Appendage (LAA) Occluder
TW: “先健科技公司”朗布爾左心耳封堵器
Taiwan·Risk Class 3·MD·LIFETECH SCIENTIFIC (SHENZHEN) CO., LTD·Registered Dec 31, 2020 – Dec 31, 2025ExpiredRegistration details
- Analysis ID
- d0dae6312c133c01ad3dd5c5c0e144e7
- License Form
- Ministry of Health Medical Device Land Transport No. 001192
- Customs Code
- DHA09200119200
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 devices
- Product Type (Level 2)
- E9999 Other
- Import Information
- Imported from abroad; Made in China
Dates and status
- Registration Date
- Dec 31, 2020
- Expiry Date
- Dec 31, 2025
About this record
Access comprehensive regulatory information for “Lifetech Scientific” LAmbre Left Atrial Appendage (LAA) Occluder in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number d0dae6312c133c01ad3dd5c5c0e144e7 and manufactured by LIFETECH SCIENTIFIC (SHENZHEN) CO., LTD. The authorized representative in Taiwan is KAISEN MEDICAL CO., LTD.
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