"Medtronic" Kleia MRI implantable cardiac rectifier defibrillator - Taiwan Registration f1d87909f5b90a6b6eaf441521845f36
Access comprehensive regulatory information for "Medtronic" Kleia MRI implantable cardiac rectifier defibrillator in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number f1d87909f5b90a6b6eaf441521845f36 and manufactured by Medtronic Inc.; Medtronic Europe Sร rl. The authorized representative in Taiwan is MEDTRONIC (TAIWAN) LTD..
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Device Details
Registration Details
f1d87909f5b90a6b6eaf441521845f36
DHA05603182205
Product Details
For details, it is Chinese approved copy of the imitation order
E Cardiovascular Medicine Science
E.3610 Pulsator of implantable cardiac rhythm apparatus
import
Dates and Status
Oct 12, 2018
Oct 12, 2028