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“TEKNIMED” NANOGEL Synthetic Bone Substitute - Taiwan Registration 94ab9c5b5e33469e6cfc7ea9c5ea17c0

Access comprehensive regulatory information for “TEKNIMED” NANOGEL Synthetic 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 94ab9c5b5e33469e6cfc7ea9c5ea17c0 and manufactured by Teknimed SAS. The authorized representative in Taiwan is GREAT UNITED STRONG ENTERPRISE CO., LTD..

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94ab9c5b5e33469e6cfc7ea9c5ea17c0
Registration Details
Taiwan FDA Registration: 94ab9c5b5e33469e6cfc7ea9c5ea17c0
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Device Details

“TEKNIMED” NANOGEL Synthetic Bone Substitute
TW: “泰克美”耐優捷凝膠人工骨泥
Risk Class 2
MD

Registration Details

94ab9c5b5e33469e6cfc7ea9c5ea17c0

Ministry of Health Medical Device Import No. 035578

DHA05603557801

Company Information

France

Product Details

Details are as detailed as approved Chinese instructions

N Orthopedics

N3045 Absorbable calcium salt bone cavity filling device

Imported from abroad

Dates and Status

Jun 10, 2022

Jun 10, 2027