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“Cadwell” ApneaTrak Sleep Diagnostic System - Taiwan Registration 60087ee78c791610bb608a14e12202ff

Access comprehensive regulatory information for “Cadwell” ApneaTrak Sleep Diagnostic System in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 60087ee78c791610bb608a14e12202ff and manufactured by CADWELL INDUSTRIES, INC.. The authorized representative in Taiwan is TRUSHINE MEDICAL INSTRUMENT 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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60087ee78c791610bb608a14e12202ff
Registration Details
Taiwan FDA Registration: 60087ee78c791610bb608a14e12202ff
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Device Details

“Cadwell” ApneaTrak Sleep Diagnostic System
TW: “凱特維爾”阿波尼亞崔克睡眠診斷系統
Risk Class 2
MD

Registration Details

60087ee78c791610bb608a14e12202ff

Ministry of Health Medical Device Import No. 035463

DHA05603546300

Company Information

United States

Product Details

Details are as detailed as approved Chinese instructions

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Dates and Status

May 05, 2022

May 05, 2027