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"Vortex" vibrating sprayer - Taiwan Registration 313e24dac8a26893dfcfde261bb038db

Access comprehensive regulatory information for "Vortex" vibrating sprayer in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 313e24dac8a26893dfcfde261bb038db and manufactured by VORTRAN MEDICAL TECHNOLOGY 1, INC.. The authorized representative in Taiwan is ASIA 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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313e24dac8a26893dfcfde261bb038db
Registration Details
Taiwan FDA Registration: 313e24dac8a26893dfcfde261bb038db
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Device Details

"Vortex" vibrating sprayer
TW: "ๆธฆๅ‚ณ"้œ‡ๅ‹•ๅผๅ™ด้œงๅ™จ
Risk Class 2
Cancelled

Registration Details

313e24dac8a26893dfcfde261bb038db

DHA00601711505

Company Information

United States

Product Details

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

D Anesthesiology

D.5905 Non-continuous respirators

import

Dates and Status

Sep 15, 2006

Sep 15, 2016

Jul 31, 2018

Cancellation Information

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