"Medtronic" Radiant Patient Program Controller - Taiwan Registration 3a57767510f4fce59cd829ea06d270b2
Access comprehensive regulatory information for "Medtronic" Radiant Patient Program Controller in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number 3a57767510f4fce59cd829ea06d270b2 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.
Device Details
Product Details
For details, it is Chinese approved copy of the imitation order
K Neuroscience
K.5840 Implantable intracranial/subdermal stimulator for pain relief
import
Dates and Status
Dec 15, 2006
Dec 15, 2011
Nov 06, 2012
Cancellation Information
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