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“COMDEK” Sleep Apnea Analysis System - Taiwan Registration a85757209253c11905cfcd69b8d81528

Access comprehensive regulatory information for “COMDEK” Sleep Apnea Analysis System in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number a85757209253c11905cfcd69b8d81528 and manufactured by COMDEK INDUSTRIAL CORPORATION. The authorized representative in Taiwan is COMDEK INDUSTRIAL CORPORATION.

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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a85757209253c11905cfcd69b8d81528
Registration Details
Taiwan FDA Registration: a85757209253c11905cfcd69b8d81528
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Device Details

“COMDEK” Sleep Apnea Analysis System
TW: “康定”睡眠呼吸分析系統
Risk Class 2
MD

Registration Details

a85757209253c11905cfcd69b8d81528

Ministry of Health Medical Device Manufacturing No. 005410

Company Information

Taiwan, Province of China

Product Details

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

D Devices for anesthesiology

D2377 Aborted Breath Monitor

Produced in Taiwan, China

Dates and Status

Jul 05, 2016

Jul 05, 2026