Taiwan FDA registration e4ab8b2125c26fc99ca76b3ddd45e2a6
"Rivanova" Reb femoral venous catheter
TW: “里凡諾瓦”雷卜股靜脈導管
Taiwan·Risk Class 2·LivaNova USA, Inc.·Registered Feb 23, 2011 – Feb 23, 2026ExpiredRegistration details
- Analysis ID
- e4ab8b2125c26fc99ca76b3ddd45e2a6
- Customs Code
- DHA00602206905
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 Medicine Science
- Product Type (Level 2)
- E.4210 Vascular catheters, cannulas and tubes for cardiopulmonary vascular bypassing
- Import Information
- import
Dates and status
- Registration Date
- Feb 23, 2011
- Expiry Date
- Feb 23, 2026
About this record
Access comprehensive regulatory information for "Rivanova" Reb femoral venous catheter in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number e4ab8b2125c26fc99ca76b3ddd45e2a6 and manufactured by LivaNova USA, Inc.. The authorized representative in Taiwan is INTERLINK MEDICAL ENTERPRISE CO., LTD..
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