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“Genoss” Polymer Guide(Non-sterile) - Taiwan Registration 583d85aba45fc6aa95b05cfeb8c48560

Access comprehensive regulatory information for “Genoss” Polymer Guide(Non-sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 583d85aba45fc6aa95b05cfeb8c48560 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. 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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583d85aba45fc6aa95b05cfeb8c48560
Registration Details
Taiwan FDA Registration: 583d85aba45fc6aa95b05cfeb8c48560
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Device Details

“Genoss” Polymer Guide(Non-sterile)
TW: “吉諾斯”牙科手術用指示器 (未滅菌)
Risk Class 1
MD
Cancelled

Registration Details

583d85aba45fc6aa95b05cfeb8c48560

Ministry of Health Medical Device Import No. 013506

DHA09401350600

Company Information

Korea, Republic of

Product Details

F Dental devices

F3980 Dental Intraosseous Implant Attachment

Imported from abroad

Dates and Status

Oct 16, 2013

Oct 16, 2023

Jun 13, 2023

Cancellation Information

Logged out

自請廢止