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"Ailang" contrast agent syringe - Taiwan Registration d5e8be5464bc7993f3030b6dd1d07124

Access comprehensive regulatory information for "Ailang" contrast agent syringe in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number d5e8be5464bc7993f3030b6dd1d07124 and manufactured by ARGON CRITICAL CARE SYSTEMS SINGAPORE PTE LTD.. The authorized representative in Taiwan is EMIND BIOTECH MR 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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d5e8be5464bc7993f3030b6dd1d07124
Registration Details
Taiwan FDA Registration: d5e8be5464bc7993f3030b6dd1d07124
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Device Details

"Ailang" contrast agent syringe
TW: โ€œๆ„›็…โ€้€ ๅฝฑๅŠ‘ๆณจๅฐ„็ญ’
Risk Class 2
Cancelled

Registration Details

d5e8be5464bc7993f3030b6dd1d07124

DHA00600959102

Company Information

Product Details

E000 of the 100,000.

import

Dates and Status

Jan 12, 2001

Jan 12, 2016

May 28, 2018

Cancellation Information

Logged out

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