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"Philips" ultrasonic system - Taiwan Registration f71d36a59ca9079e7e96b295e4c58cf0

Access comprehensive regulatory information for "Philips" ultrasonic system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number f71d36a59ca9079e7e96b295e4c58cf0 and manufactured by Philips Healthcare (Suzhou) Co., Ltd. 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 ULTRASOUND, INC., Philips Ultrasound, LLC, 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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f71d36a59ca9079e7e96b295e4c58cf0
Registration Details
Taiwan FDA Registration: f71d36a59ca9079e7e96b295e4c58cf0
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Device Details

"Philips" ultrasonic system
TW: โ€œ้ฃ›ๅˆฉๆตฆโ€่ถ…้Ÿณๆณข็ณป็ตฑ
Risk Class 2
Cancelled

Registration Details

f71d36a59ca9079e7e96b295e4c58cf0

DHA09200070702

Company Information

Product Details

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

P Radiology Science

P.1550 Ultrasonic pulsating Duppler imaging system

Input;; Chinese goods

Dates and Status

Oct 08, 2015

Oct 08, 2020

Jul 15, 2022

Cancellation Information

Logged out

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