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"Bard" Apt balloon expansion catheter - Taiwan Registration 8b50f7b8fca8de5880fa5850b123b08f

Access comprehensive regulatory information for "Bard" Apt balloon expansion catheter in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 8b50f7b8fca8de5880fa5850b123b08f 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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8b50f7b8fca8de5880fa5850b123b08f
Registration Details
Taiwan FDA Registration: 8b50f7b8fca8de5880fa5850b123b08f
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Device Details

"Bard" Apt balloon expansion catheter
TW: โ€œๅทดๅพทโ€่‰พๆ™ฎ็‰นๆฐฃ็ƒๆ“ดๅผตๅฐŽ็ฎก
Risk Class 2
Cancelled

Registration Details

8b50f7b8fca8de5880fa5850b123b08f

DHA00602017701

Company Information

United States

Product Details

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

E Cardiovascular Medicine Science

E.1250 Percutaneous catheters

import

Dates and Status

Sep 16, 2009

Sep 16, 2014

May 28, 2018

Cancellation Information

Logged out

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