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"Medtronic" Keneng titanium-coated intervertebral fusion system - Taiwan Registration e4c8553d01239617f2ec8d07163c858f

Access comprehensive regulatory information for "Medtronic" Keneng titanium-coated intervertebral fusion system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number e4c8553d01239617f2ec8d07163c858f and manufactured by MEDTRONIC SOFAMOR DANEK DEGGENDORF GMBH;; MEDTRONIC SOFAMOR DANEK USA, INC.. The authorized representative in Taiwan is MEDTRONIC (TAIWAN) LTD..

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e4c8553d01239617f2ec8d07163c858f
Registration Details
Taiwan FDA Registration: e4c8553d01239617f2ec8d07163c858f
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Device Details

"Medtronic" Keneng titanium-coated intervertebral fusion system
TW: โ€œ็พŽๆ•ฆๅŠ›โ€็ง‘่ƒฝ้ˆฆๅก—ๅฑคๆคŽ้–“่žๅˆ็ณป็ตฑ
Risk Class 2

Registration Details

e4c8553d01239617f2ec8d07163c858f

DHA05603223100

Company Information

Product Details

For details, it is Chinese approved copy of the imitation order

N Orthopedics

N.3080 ๆคŽ้ซ”้–“่žๅˆ่ฃ็ฝฎ

import

Dates and Status

Jan 29, 2019

Jan 29, 2029