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"Medtronic" Aseanda implantable spinal cord endoluminal catheter - Taiwan Registration e8dda693a94196a0b521c309c032db93

Access comprehensive regulatory information for "Medtronic" Aseanda implantable spinal cord 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 e8dda693a94196a0b521c309c032db93 and manufactured by Medtronic Puerto Rico Operations Co., Juncos;; Medtronic Inc.. The authorized representative in Taiwan is MEDTRONIC (TAIWAN) LTD..

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e8dda693a94196a0b521c309c032db93
Registration Details
Taiwan FDA Registration: e8dda693a94196a0b521c309c032db93
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Device Details

"Medtronic" Aseanda implantable spinal cord endoluminal catheter
TW: โ€œ็พŽๆ•ฆๅŠ›โ€ไบžๅ–„้”ๆคๅ…ฅๅผ่„Š้ซ“่…”ๅ…งๅฐŽ็ฎก
Risk Class 3

Registration Details

e8dda693a94196a0b521c309c032db93

DHA05603259104

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

May 02, 2019

May 02, 2029