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"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..

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3a57767510f4fce59cd829ea06d270b2
Registration Details
Taiwan FDA Registration: 3a57767510f4fce59cd829ea06d270b2
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Device Details

"Medtronic" Radiant Patient Program Controller
TW: "็พŽๆ•ฆๅŠ›"่‰พ็’€็—…ๆ‚ฃ็จ‹ๆŽงๅ„€
Risk Class 3
Cancelled

Registration Details

3a57767510f4fce59cd829ea06d270b2

DHA00601751406

Company Information

United States

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

Logged out

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