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"Shi Kyūki" Zenshin Repair Supplementary Bone Substitute - Taiwan Registration 26287087b945088c86aab877d86aeef4

Access comprehensive regulatory information for "Shi Kyūki" Zenshin Repair Supplementary Bone Substitute in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 26287087b945088c86aab877d86aeef4 and manufactured by SMITH & NEPHEW, INC., ENDOSCOPY DIVISION. The authorized representative in Taiwan is SMITH & NEPHEW ( OVERSEAS ) LIMITED, TAIWAN BRANCH (U.K.).

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26287087b945088c86aab877d86aeef4
Registration Details
Taiwan FDA Registration: 26287087b945088c86aab877d86aeef4
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Device Details

"Shi Kyūki" Zenshin Repair Supplementary Bone Substitute
TW: “史耐輝”全真修補骨代替物
Risk Class 2
Cancelled

Registration Details

26287087b945088c86aab877d86aeef4

DHA00602009904

Company Information

Product Details

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

N Orthopedics

import

Dates and Status

Aug 06, 2009

Aug 06, 2014

Jun 25, 2018

Cancellation Information

Logged out

許可證已逾有效期