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“Fisher&Paykel” SleepStyle CPAP system - Taiwan Registration eb5296e4dea2ebfa21f996bc72beefb6

Access comprehensive regulatory information for “Fisher&Paykel” SleepStyle CPAP system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number eb5296e4dea2ebfa21f996bc72beefb6 and manufactured by FISHER & PAYKEL HEALTHCARE LTD.. The authorized representative in Taiwan is FISHER & PAYKEL HEALTHCARE ASIA LIMITED, TAIWAN BRANCH (NEW ZEALAND).

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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eb5296e4dea2ebfa21f996bc72beefb6
Registration Details
Taiwan FDA Registration: eb5296e4dea2ebfa21f996bc72beefb6
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Device Details

“Fisher&Paykel” SleepStyle CPAP system
TW: “費雪派克”正壓呼吸輔助器
Risk Class 2
MD

Registration Details

eb5296e4dea2ebfa21f996bc72beefb6

Ministry of Health Medical Device Import No. 031831

DHA05603183106

Company Information

Product Details

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

D Devices for anesthesiology

D5905 Discontinuous respirators

Imported from abroad

Dates and Status

Oct 22, 2018

Oct 22, 2028