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"Medtronic" Keneng spine system device - Taiwan Registration 7c41aceebd6d9682f616db292b6f7684

Access comprehensive regulatory information for "Medtronic" Keneng spine system device in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 7c41aceebd6d9682f616db292b6f7684 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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7c41aceebd6d9682f616db292b6f7684
Registration Details
Taiwan FDA Registration: 7c41aceebd6d9682f616db292b6f7684
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Device Details

"Medtronic" Keneng spine system device
TW: โ€œ็พŽๆ•ฆๅŠ›โ€็ง‘่ƒฝ่„ŠๆคŽ็ณป็ตฑ่ฃ็ฝฎ
Risk Class 2

Registration Details

7c41aceebd6d9682f616db292b6f7684

DHA00602443208

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 10, 2013

Jan 10, 2028