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Philips patient monitoring system - Taiwan Registration fa38b2e7a79455d769c047e58bbdf959

Access comprehensive regulatory information for Philips patient monitoring system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number fa38b2e7a79455d769c047e58bbdf959 and manufactured by INVIVO CORPORATION. The authorized representative in Taiwan is PHILIPS TAIWAN LIMITED.

This page provides complete technical specifications, regulatory compliance details. 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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fa38b2e7a79455d769c047e58bbdf959
Registration Details
Taiwan FDA Registration: fa38b2e7a79455d769c047e58bbdf959
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Device Details

Philips patient monitoring system
TW: โ€œ้ฃ›ๅˆฉๆตฆโ€็—…ๆ‚ฃ็›ฃ่ฆ–็ณป็ตฑ
Risk Class 3
Cancelled

Registration Details

fa38b2e7a79455d769c047e58bbdf959

DHA00602246602

Company Information

United States

Product Details

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

E Cardiovascular Medicine Science

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

import

Dates and Status

Jul 11, 2011

Jul 11, 2016

Apr 25, 2018

Cancellation Information

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