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"Philips" ultrasonic system - Taiwan Registration 892f3ddc3a216e81188d27f777156959

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 892f3ddc3a216e81188d27f777156959 and manufactured by PHILIPS ULTRASOUND, INC.. 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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892f3ddc3a216e81188d27f777156959
Registration Details
Taiwan FDA Registration: 892f3ddc3a216e81188d27f777156959
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Device Details

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

Registration Details

892f3ddc3a216e81188d27f777156959

DHA00602396601

Company Information

United States

Product Details

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

P Radiology Science

P.1560 ่ถ…้Ÿณๆณขๅ›ž้Ÿณๅฝฑๅƒ็ณป็ตฑ

import

Dates and Status

Sep 19, 2012

Sep 19, 2017

Dec 13, 2019

Cancellation Information

Logged out

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