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"Philips" delivery room information management system - Taiwan Registration 3834ed0a849a06c31de819346894c870

Access comprehensive regulatory information for "Philips" delivery room information management system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 3834ed0a849a06c31de819346894c870 and manufactured by PHILIPS MEDICAL SYSTEMS. The authorized representative in Taiwan is PHILIPS TAIWAN LIMITED.

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including PHILIPS MEDICAL SYSTEMS, and 2 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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3834ed0a849a06c31de819346894c870
Registration Details
Taiwan FDA Registration: 3834ed0a849a06c31de819346894c870
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Device Details

"Philips" delivery room information management system
TW: โ€œ้ฃ›ๅˆฉๆตฆโ€็”ขๆˆฟ่ณ‡่จŠ็ฎก็†็ณป็ตฑ
Risk Class 2
Cancelled

Registration Details

3834ed0a849a06c31de819346894c870

DHA00602070000

Company Information

United States

Product Details

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

l Obstetrics and Gynecology

L.2740 Pre- and post-production monitoring systems and accessories

import

Dates and Status

Mar 24, 2010

Mar 24, 2015

Apr 25, 2018

Cancellation Information

Logged out

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