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"Vortex" automatic wake-up device - Taiwan Registration c327485e9e7151ed5b5c47cb39e87e1e

Access comprehensive regulatory information for "Vortex" automatic wake-up device in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number c327485e9e7151ed5b5c47cb39e87e1e 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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c327485e9e7151ed5b5c47cb39e87e1e
Registration Details
Taiwan FDA Registration: c327485e9e7151ed5b5c47cb39e87e1e
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Device Details

"Vortex" automatic wake-up device
TW: "ๆธฆๅ‚ณ"่‡ชๅ‹•็”ฆ้†’ๅ™จ
Risk Class 2
Cancelled

Registration Details

c327485e9e7151ed5b5c47cb39e87e1e

DHA00601710604

Company Information

United States

Product Details

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

D Anesthesiology

D.5925 Powered emergency breathing apparatus

import

Dates and Status

Sep 12, 2006

Sep 12, 2016

Jul 31, 2018

Cancellation Information

Logged out

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