Taiwan FDA registration 64660cbee8b5be8783013e4187c96066
“LivaNova” FlexFlow Venous Cannula
TW: “里凡諾瓦”菲樂流靜脈導管
Taiwan·Risk Class 2·MD·LivaNova USA, Inc.·Registered May 28, 2015 – May 28, 2025ExpiredRegistration details
- Analysis ID
- 64660cbee8b5be8783013e4187c96066
- License Form
- Ministry of Health Medical Device Import No. 027310
- Customs Code
- DHA05602731002
Company information
- Manufacturer
- LivaNova USA, Inc.
- Manufacturer Country
- United States
- Authorized Representative
- INTERLINK MEDICAL ENTERPRISE 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)
- E4210 Vascular catheters, cannula and tubes for cardiopulmonary vascular bypass
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- May 28, 2015
- Expiry Date
- May 28, 2025
About this record
Access comprehensive regulatory information for “LivaNova” FlexFlow Venous Cannula in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 64660cbee8b5be8783013e4187c96066 and manufactured by LivaNova USA, Inc.. The authorized representative in Taiwan is INTERLINK MEDICAL ENTERPRISE CO., LTD..
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