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“Bard” Vacora Vacuum Assisted Biopsy System Accessories - Taiwan Registration 05e7cb5e1fd35eee6dd7a8b20e552265

Access comprehensive regulatory information for “Bard” Vacora Vacuum Assisted Biopsy System Accessories in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 05e7cb5e1fd35eee6dd7a8b20e552265 and manufactured by BARD PERIPHERAL VASCULAR, INC.. The authorized representative in Taiwan is BARD PACIFIC HEALTH CARE CO., LTD..

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05e7cb5e1fd35eee6dd7a8b20e552265
Registration Details
Taiwan FDA Registration: 05e7cb5e1fd35eee6dd7a8b20e552265
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Device Details

“Bard” Vacora Vacuum Assisted Biopsy System Accessories
TW: “巴德”維可拉真空輔助組織取樣系統配件
Risk Class 2
MD

Registration Details

05e7cb5e1fd35eee6dd7a8b20e552265

Ministry of Health Medical Device Import No. 029230

DHA05602923001

Company Information

United States

Product Details

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

H Gastroenterology-urology devices

H1075 Gastroenterology - Urology biopsy instruments

Imported from abroad

Dates and Status

Dec 26, 2016

Dec 26, 2026