Taiwan FDA registration f0099f666cb296dd282b3083a031a0c3
"Lifetech Technology Company" Shri elastic interatrial septal 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 (Europe) Coöperatief U.A.·Registered Sep 06, 2024 – Jul 12, 2029ActiveRegistration details
- Analysis ID
- f0099f666cb296dd282b3083a031a0c3
- Customs Code
- DHA05603729805
Company information
- Manufacturer
- LifeTech Scientific (Europe) Coöperatief U.A.
- Manufacturer Country
- Netherlands
- Authorized Representative
- KAISEN MEDICAL CO., LTD
Product details
- Intended Use
- Details are as detailed as approved Chinese instructions
- Product Type (Level 1)
- E Cardiovascular Medicine Science
- Product Type (Level 2)
- E.9999 Miscellaneous
- Import Information
- import
Dates and status
- Registration Date
- Sep 06, 2024
- Expiry Date
- Jul 12, 2029
About this record
Access comprehensive regulatory information for "Lifetech Technology Company" Shri elastic interatrial septal occluder in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number f0099f666cb296dd282b3083a031a0c3 and manufactured by LifeTech Scientific (Europe) Coöperatief U.A.. The authorized representative in Taiwan is KAISEN MEDICAL CO., LTD.
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