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"Philips" ultrasonic system - Taiwan Registration bac592f37bf75fdc285640f669a21185

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 bac592f37bf75fdc285640f669a21185 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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bac592f37bf75fdc285640f669a21185
Registration Details
Taiwan FDA Registration: bac592f37bf75fdc285640f669a21185
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Device Details

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

Registration Details

bac592f37bf75fdc285640f669a21185

DHA00602391500

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

Aug 01, 2012

Aug 01, 2027