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"Leishi" multiple sleep physiology recorder - Taiwan Registration 856ea1e4c5500848f65d102a960dcef1

Access comprehensive regulatory information for "Leishi" multiple sleep physiology recorder in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 856ea1e4c5500848f65d102a960dcef1 and manufactured by RESPIRONICS INC.. The authorized representative in Taiwan is PHILIPS TAIWAN LIMITED.

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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856ea1e4c5500848f65d102a960dcef1
Registration Details
Taiwan FDA Registration: 856ea1e4c5500848f65d102a960dcef1
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Device Details

"Leishi" multiple sleep physiology recorder
TW: โ€œ็ฃŠไป•โ€ๅคš้‡็ก็œ ็”Ÿ็†่จ˜้Œ„ๅ„€
Risk Class 2

Registration Details

856ea1e4c5500848f65d102a960dcef1

DHA00602326204

Company Information

United States

Product Details

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

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import

Dates and Status

Feb 20, 2012

Feb 20, 2027