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“Genoss” Osteon - Taiwan Registration b591e09acb94c427f6540c09ba08041c

Access comprehensive regulatory information for “Genoss” Osteon in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number b591e09acb94c427f6540c09ba08041c and manufactured by Genoss Co., Ltd.. The authorized representative in Taiwan is MRS MICRO-WORK COMPANY LIMITED.

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including Genoss Co., Ltd., and 1 recent registrations in the same category. 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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b591e09acb94c427f6540c09ba08041c
Registration Details
Taiwan FDA Registration: b591e09acb94c427f6540c09ba08041c
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Device Details

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

Registration Details

b591e09acb94c427f6540c09ba08041c

Ministry of Health Medical Device Import No. 026185

DHA05602618507

Company Information

Korea, Republic of

Product Details

F Dental devices

F3930 Tricalcium phosphate for alveolar bone restoration

Imported from abroad

Dates and Status

May 29, 2014

May 29, 2024

Jun 05, 2023

Cancellation Information

Logged out

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