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"Sindis" new generation of Xinkeji intervertebral stent implant - Taiwan Registration 06f900b7256170a2aa7fb7c6e2c0a928

Access comprehensive regulatory information for "Sindis" new generation of Xinkeji intervertebral stent implant in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 06f900b7256170a2aa7fb7c6e2c0a928 and manufactured by SYNTHES GMBH;; Jabil Switzerland Manufacturing GmbH. The authorized representative in Taiwan is JOHNSON & JOHNSON MEDICAL TAIWAN LTD..

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06f900b7256170a2aa7fb7c6e2c0a928
Registration Details
Taiwan FDA Registration: 06f900b7256170a2aa7fb7c6e2c0a928
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Device Details

"Sindis" new generation of Xinkeji intervertebral stent implant
TW: โ€œไฟก่ฟชๆ€โ€ๆ–ฐไธ€ไปฃ่พ›ๅ‡ฑๅ‰ๆคŽ้–“ๆ”ฏๆžถๆคๅ…ฅ็‰ฉ
Risk Class 2

Registration Details

06f900b7256170a2aa7fb7c6e2c0a928

DHA05603251909

Company Information

Product Details

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

N Orthopedics

N.3080 ๆคŽ้ซ”้–“่žๅˆ่ฃ็ฝฎ

Input;; Contract manufacturing

Dates and Status

Apr 19, 2019

Apr 19, 2029