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“Bard” Totalis Flexible Endo Kit - Taiwan Registration 13adc7795e1f00603f89f2db3df579f8

Access comprehensive regulatory information for “Bard” Totalis Flexible Endo Kit in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 13adc7795e1f00603f89f2db3df579f8 and manufactured by C.R. BARD, INC.. The authorized representative in Taiwan is BARD PACIFIC HEALTH CARE 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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13adc7795e1f00603f89f2db3df579f8
Registration Details
Taiwan FDA Registration: 13adc7795e1f00603f89f2db3df579f8
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Device Details

“Bard” Totalis Flexible Endo Kit
TW: “巴德”同達力斯可彎曲式泌尿科內視鏡套件
Risk Class 2
MD

Registration Details

13adc7795e1f00603f89f2db3df579f8

Ministry of Health Medical Device Import No. 029355

DHA05602935508

Company Information

United States

Product Details

For details, it is Chinese approved copy of the imitation order

H Gastroenterology-urology devices

H4620 Ureteral stents

Imported from abroad

Dates and Status

Jan 26, 2017

Jan 26, 2022