"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
Device Details
"Leishi" multiple sleep physiology recorder
TW: โ็ฃไปโๅค้็ก็ ็็่จ้ๅ
Risk Class 2

