"Leishi" physiological recorder - Taiwan Registration bf0ecd4d53f622806a4e664ac28e795f
Access comprehensive regulatory information for "Leishi" physiological recorder in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number bf0ecd4d53f622806a4e664ac28e795f and manufactured by Kimball Electronics Group LLC- Jasper;; 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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bf0ecd4d53f622806a4e664ac28e795f
Registration Details
Taiwan FDA Registration: bf0ecd4d53f622806a4e664ac28e795f
Device Details
"Leishi" physiological recorder
TW: โ็ฃไปโ็็่จ้ๅ
Risk Class 2

