"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
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

