Taiwan FDA registration 1cdb3df543b2f7da0cecc097f785a342

"Medtronic" Interles programmaster app

TW: “美敦力” 因特列斯程控儀應用程式

Taiwan·Risk Class 3·MEDTRONIC NEUROMODULATION·Registered May 07, 2020 – May 07, 2030Active

Registration details

Analysis ID: 1cdb3df543b2f7da0cecc097f785a342
Customs Code: DHA05603341005

Company information

Manufacturer: MEDTRONIC NEUROMODULATION
Manufacturer Country: United States
Authorized Representative: MEDTRONIC (TAIWAN) LTD.

Product details

Intended Use: Neurostimulators (extracorporeal or implantable) used by clinicians to program-control the following Medtronic pain treatments: In Vitro: Model 97725 Wireless Extracorporeal Neurostimulator. Implantable: Model 97715 AdaptiveStim technology and SureScan MRI technology Interles implantable neurostimulator, Model 97716 Intramax implantable neurostimulator with SureScan MRI technology.
Product Type (Level 1): K Neuroscience
Product Type (Level 2): K.5880 Implantable spinal cord stimulator for pain relief
Import Information: import

Dates and status

Registration Date: May 07, 2020
Expiry Date: May 07, 2030

About this record

Access comprehensive regulatory information for "Medtronic" Interles programmaster app in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number 1cdb3df543b2f7da0cecc097f785a342 and manufactured by MEDTRONIC NEUROMODULATION. The authorized representative in Taiwan is MEDTRONIC (TAIWAN) LTD..

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