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“Bard” Proxis Ureteral Access Sheath - Taiwan Registration 8f7ee0c4f510f41f796be5fe3a53b407

Access comprehensive regulatory information for “Bard” Proxis Ureteral Access Sheath in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 8f7ee0c4f510f41f796be5fe3a53b407 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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8f7ee0c4f510f41f796be5fe3a53b407
Registration Details
Taiwan FDA Registration: 8f7ee0c4f510f41f796be5fe3a53b407
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Device Details

“Bard” Proxis Ureteral Access Sheath
TW: “巴德”波瑟斯輸尿管通路導尿管鞘
Risk Class 2
MD

Registration Details

8f7ee0c4f510f41f796be5fe3a53b407

Ministry of Health Medical Device Import No. 032348

DHA05603234808

Company Information

United States

Product Details

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

H Gastroenterology-urology devices

H1500 endoscope and accessories

Imported from abroad

Dates and Status

Mar 24, 2019

Mar 24, 2024