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"Philips" ultrasonic system - Taiwan Registration d51ab98c6acf7179b08eed83024e62f3

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 d51ab98c6acf7179b08eed83024e62f3 and manufactured by Philips Healthcare (Suzhou) Co., Ltd;; Philips Ultrasound, LLC. 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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d51ab98c6acf7179b08eed83024e62f3
Registration Details
Taiwan FDA Registration: d51ab98c6acf7179b08eed83024e62f3
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Device Details

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

Registration Details

d51ab98c6acf7179b08eed83024e62f3

DHA09200081107

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

Chinese goods;; input

Dates and Status

Jan 10, 2017

Sep 11, 2027