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"Philips" patient monitor - Taiwan Registration 92002cbbee69caf749f52cabd6564d8b

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 92002cbbee69caf749f52cabd6564d8b 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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92002cbbee69caf749f52cabd6564d8b
Registration Details
Taiwan FDA Registration: 92002cbbee69caf749f52cabd6564d8b
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Device Details

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

Registration Details

92002cbbee69caf749f52cabd6564d8b

DHA09200097804

Company Information

Product Details

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

E Cardiovascular Medicine Science

Input;; Chinese goods

Dates and Status

Feb 19, 2019

Feb 19, 2029