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"Philips" ultrasonic system - Taiwan Registration d8531afe8fcc24d9c51836b94fa7588a

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 d8531afe8fcc24d9c51836b94fa7588a 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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d8531afe8fcc24d9c51836b94fa7588a
Registration Details
Taiwan FDA Registration: d8531afe8fcc24d9c51836b94fa7588a
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Device Details

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

Registration Details

d8531afe8fcc24d9c51836b94fa7588a

DHA05603324401

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

Feb 18, 2020

Feb 18, 2030