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"Philips" patient monitor - Taiwan Registration d3be6f859582a02e508310b4f66c80cb

Access comprehensive regulatory information for "Philips" patient monitor in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number d3be6f859582a02e508310b4f66c80cb and manufactured by Philips Goldway (Shenzhen) Industrial Inc.. The authorized representative in Taiwan is PHILIPS TAIWAN LIMITED.

This page provides complete technical specifications, regulatory compliance details, 5 companies making similar products including PHILIPS MEDIZINSYSTEME Bร–BLINGEN GMBH, PHILIPS MEDICAL SYSTEMS, and 5 recent registrations in the same category. 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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d3be6f859582a02e508310b4f66c80cb
Registration Details
Taiwan FDA Registration: d3be6f859582a02e508310b4f66c80cb
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Device Details

"Philips" patient monitor
TW: โ€œ้ฃ›ๅˆฉๆตฆโ€ ็—…ๆ‚ฃ็›ฃ่ฆ–ๅ™จ
Risk Class 2

Registration Details

d3be6f859582a02e508310b4f66c80cb

DHA09200126804

Company Information

Product Details

Details are as detailed as approved Chinese instructions

E Cardiovascular Medicine Science

E.2300 Cardiac monitor (including cardiac data and heart rate monitor)

Input;; Chinese goods

Dates and Status

Nov 09, 2021

Nov 09, 2026