Pure Global

"Philips" patient monitor - Taiwan Registration 002c545656ad8fb08c1d10e63426392c

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 002c545656ad8fb08c1d10e63426392c and manufactured by ;; PHILIPS MEDIZIN SYSTEME BOEBLINGEN GMBH. The authorized representative in Taiwan is PHILIPS TAIWAN LIMITED.

This page provides complete technical specifications, regulatory compliance details, 4 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.

Free Database
Powered by Pure Global AI
89,000+ Devices
4 Competitors
5 Recent Registrations
002c545656ad8fb08c1d10e63426392c
Registration Details
Taiwan FDA Registration: 002c545656ad8fb08c1d10e63426392c
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing

Device Details

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

Registration Details

002c545656ad8fb08c1d10e63426392c

DHA05603153502

Company Information

Product Details

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

E Cardiovascular Medicine Science

E.1025 Arrhythmia Detectors and Alerts

import

Dates and Status

Sep 27, 2018

Sep 27, 2028