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Honeytec balloon dilation catheter - Taiwan Registration 8c6175146fe331de6bab2af1b55c494c

Access comprehensive regulatory information for Honeytec balloon dilation catheter in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 8c6175146fe331de6bab2af1b55c494c and manufactured by BARD PERIPHERAL VASCULAR, INC.;; CLEARSTREAM TECHNOLOGIES LTD.. 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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8c6175146fe331de6bab2af1b55c494c
Registration Details
Taiwan FDA Registration: 8c6175146fe331de6bab2af1b55c494c
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Device Details

Honeytec balloon dilation catheter
TW: ๆ‚่€ๅพ—็ƒๅ›Šๆ“ดๅผตๅฐŽ็ฎก
Risk Class 2

Registration Details

8c6175146fe331de6bab2af1b55c494c

DHA05603723000

Company Information

Product Details

Details are as detailed as approved Chinese instructions

E Cardiovascular Medicine Science

E.1250 Percutaneous catheters

import

Dates and Status

Jun 25, 2024

Jun 25, 2029