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"Philips" patient monitor - Taiwan Registration 1b49323e65cdfd5d02310586c21fa00b

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 1b49323e65cdfd5d02310586c21fa00b and manufactured by PHILIPS MEDIZINSYSTEME BÖBLINGEN GMBH. 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 MEDICAL SYSTEMS, PHILIPS MEDIZINSYSTEME BÖBLINGEN GMBH, 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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1b49323e65cdfd5d02310586c21fa00b
Registration Details
Taiwan FDA Registration: 1b49323e65cdfd5d02310586c21fa00b
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Device Details

"Philips" patient monitor
TW: “飛利浦”病患監視器
Risk Class 2

Registration Details

1b49323e65cdfd5d02310586c21fa00b

DHA00602425104

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

Dec 12, 2012

Dec 12, 2027