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"Philips" patient monitor - Taiwan Registration e7f858d0c3f2dae1de83742bcf680d9c

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 e7f858d0c3f2dae1de83742bcf680d9c 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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e7f858d0c3f2dae1de83742bcf680d9c
Registration Details
Taiwan FDA Registration: e7f858d0c3f2dae1de83742bcf680d9c
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Device Details

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

Registration Details

e7f858d0c3f2dae1de83742bcf680d9c

DHA00602394802

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 06, 2012

Sep 06, 2022

Apr 12, 2024

Cancellation Information

Logged out

許可證已逾有效期