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"Philips" ultrasonic system - Taiwan Registration 29a0f6a5cb4bc420ca7afc09f535edf2

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 29a0f6a5cb4bc420ca7afc09f535edf2 and manufactured by 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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29a0f6a5cb4bc420ca7afc09f535edf2
Registration Details
Taiwan FDA Registration: 29a0f6a5cb4bc420ca7afc09f535edf2
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Device Details

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

Registration Details

29a0f6a5cb4bc420ca7afc09f535edf2

DHA05603333800

Company Information

United States

Product Details

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

P Radiology Science

P.1550 Ultrasonic pulsating Duppler imaging system

import

Dates and Status

Mar 30, 2020

Mar 30, 2030