Pure Global

"Medtronic" spinal endoluminal catheter - Taiwan Registration 876443cc42192a1db21edcc0b18136b6

Access comprehensive regulatory information for "Medtronic" spinal endoluminal catheter in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number 876443cc42192a1db21edcc0b18136b6 and manufactured by Medtronic Puerto Rico Operations Co., Juncos;; Medtronic Inc.. 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
876443cc42192a1db21edcc0b18136b6
Registration Details
Taiwan FDA Registration: 876443cc42192a1db21edcc0b18136b6
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing

Device Details

"Medtronic" spinal endoluminal catheter
TW: โ€œ็พŽๆ•ฆๅŠ›โ€ ่„Š้ซ“่…”ๅ…งๅฐŽ็ฎก
Risk Class 3

Registration Details

876443cc42192a1db21edcc0b18136b6

DHA05602557301

Company Information

Product Details

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

J General hospital and personal use equipment

J.9999 Miscellaneous

import

Dates and Status

Nov 04, 2013

Nov 04, 2023