“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..
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.
Device Details
Registration Details
05e7cb5e1fd35eee6dd7a8b20e552265
Ministry of Health Medical Device Import No. 029230
DHA05602923001
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

