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“Applied”GelPOINT V-Path Transvaginal Access Platform - Taiwan Registration 972c2a50b5987307afe31abd2e9a1bcd

Access comprehensive regulatory information for “Applied”GelPOINT V-Path Transvaginal Access Platform in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 972c2a50b5987307afe31abd2e9a1bcd and manufactured by APPLIED MEDICAL RESOURCES CORPORATION. The authorized representative in Taiwan is DOUBLE-SUCCESS CO., LTD..

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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972c2a50b5987307afe31abd2e9a1bcd
Registration Details
Taiwan FDA Registration: 972c2a50b5987307afe31abd2e9a1bcd
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Device Details

“Applied”GelPOINT V-Path Transvaginal Access Platform
TW: “安培”經陰道手術通路
Risk Class 2
MD

Registration Details

972c2a50b5987307afe31abd2e9a1bcd

Ministry of Health Medical Device Import No. 035768

DHA05603576806

Company Information

United States

Product Details

Details are as detailed as approved Chinese instructions

l Obstetrics and Gynecology

L1640 recessed mirror and accessories

Imported from abroad

Dates and Status

Aug 25, 2022

Aug 25, 2027