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“Genoss” Osteon 3 - Taiwan Registration a65d4d9c036d3b1086683af815b56a53

Access comprehensive regulatory information for “Genoss” Osteon 3 in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number a65d4d9c036d3b1086683af815b56a53 and manufactured by Genoss Co., Ltd.. The authorized representative in Taiwan is QUALTECH CONSULTING CORPORATION.

This page provides complete technical specifications, regulatory compliance details. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.

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a65d4d9c036d3b1086683af815b56a53
Registration Details
Taiwan FDA Registration: a65d4d9c036d3b1086683af815b56a53
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Device Details

“Genoss” Osteon 3
TW: “吉諾斯”牙科骨粉
Risk Class 2
MD

Registration Details

a65d4d9c036d3b1086683af815b56a53

Ministry of Health Medical Device Import No. 035295

DHA05603529502

Company Information

Korea, Republic of

Product Details

Details are as detailed as approved Chinese instructions

F Dentistry

F3930 Alveolar Restoration Materials

Imported from abroad

Dates and Status

Mar 14, 2022

Mar 14, 2027