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"Figon" ultra-light preterm infant central venous catheter - Taiwan Registration acdd2f1816445f84f794c9f8920712ce

Access comprehensive regulatory information for "Figon" ultra-light preterm infant central venous catheter in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number acdd2f1816445f84f794c9f8920712ce and manufactured by VYGON. The authorized representative in Taiwan is TRIPLE ROPES ENTERPRISE 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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acdd2f1816445f84f794c9f8920712ce
Registration Details
Taiwan FDA Registration: acdd2f1816445f84f794c9f8920712ce
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Device Details

"Figon" ultra-light preterm infant central venous catheter
TW: โ€œๆ–่ฒขโ€่ถ…่ผ•ๆ—ฉ็”ขๅ…’ไธญๅคฎ้œ่„ˆๅฐŽ็ฎก
Risk Class 2
Cancelled

Registration Details

acdd2f1816445f84f794c9f8920712ce

DHA00601962308

Company Information

France

Product Details

It is designed for very low birth weight prematures (VLBW) weighing less than 800 grams and can be visualized on X-ray. It is a polyureamine catheter inserted from a peripheral vein that can be administered and nourished for a long time.

E Cardiovascular Medicine Science

E.1250 Percutaneous catheters

import

Dates and Status

Dec 23, 2008

Dec 23, 2013

Apr 24, 2015

Cancellation Information

Logged out

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