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“Bard” Magnum Reusable Core Biopsy Instrument - Taiwan Registration 4e666af17b1e8a2e53879bd45c108b9a

Access comprehensive regulatory information for “Bard” Magnum Reusable Core Biopsy Instrument in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 4e666af17b1e8a2e53879bd45c108b9a 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.

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4e666af17b1e8a2e53879bd45c108b9a
Registration Details
Taiwan FDA Registration: 4e666af17b1e8a2e53879bd45c108b9a
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Device Details

“Bard” Magnum Reusable Core Biopsy Instrument
TW: “巴德”瑪格寧可重複使用式核心取樣器械
Risk Class 2
MD

Registration Details

4e666af17b1e8a2e53879bd45c108b9a

Ministry of Health Medical Device Import No. 029895

DHA05602989501

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

Jun 07, 2017

Jun 07, 2027