Pure Global

"Medtronic" vascular catheter - Taiwan Registration 87e7d0a7496790c1e7eb59f237ce9dbe

Access comprehensive regulatory information for "Medtronic" vascular catheter in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 87e7d0a7496790c1e7eb59f237ce9dbe and manufactured by MEDTRONIC NEUROMODULATION. The authorized representative in Taiwan is MEDTRONIC (TAIWAN) 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
87e7d0a7496790c1e7eb59f237ce9dbe
Registration Details
Taiwan FDA Registration: 87e7d0a7496790c1e7eb59f237ce9dbe
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing

Device Details

"Medtronic" vascular catheter
TW: "็พŽๆ•ฆๅŠ›"่ก€็ฎกๅฐŽ็ฎก
Risk Class 2
Cancelled

Registration Details

87e7d0a7496790c1e7eb59f237ce9dbe

DHA00601165405

Company Information

United States

Product Details

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

J General hospital and personal use equipment

J.5970 Percutaneous long-term implantable endovascular catheters

import

Dates and Status

Aug 04, 2005

Aug 04, 2015

Apr 25, 2018

Cancellation Information

Logged out

่‡ช่กŒ้ตๅ…ฅ