Pure Global

"Rivanova" puncture set - Taiwan Registration e880d8788bd7b9656603be44608d03c8

Access comprehensive regulatory information for "Rivanova" puncture set in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number e880d8788bd7b9656603be44608d03c8 and manufactured by LivaNova USA, Inc.. The authorized representative in Taiwan is INTERLINK MEDICAL ENTERPRISE 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 Database
Powered by Pure Global AI
89,000+ Devices
e880d8788bd7b9656603be44608d03c8
Registration Details
Taiwan FDA Registration: e880d8788bd7b9656603be44608d03c8
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing

Device Details

"Rivanova" puncture set
TW: โ€œ้‡Œๅ‡ก่ซพ็“ฆโ€็ฉฟๅˆบๅฅ—็ต„
Risk Class 2

Registration Details

e880d8788bd7b9656603be44608d03c8

DHA05602731104

Company Information

United States

Product Details

For details, it is Chinese approved copy of the imitation order

E Cardiovascular Medicine Science

E.4210 Vascular catheters, cannulas and tubes for cardiopulmonary vascular bypassing

import

Dates and Status

May 28, 2015

May 28, 2030