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"Philips" ultrasonic system - Taiwan Registration 30d29dbd82666e800adf30d0249b8ab5

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 30d29dbd82666e800adf30d0249b8ab5 and manufactured by PHILIPS ULTRASOUND. 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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30d29dbd82666e800adf30d0249b8ab5
Registration Details
Taiwan FDA Registration: 30d29dbd82666e800adf30d0249b8ab5
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Device Details

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

Registration Details

30d29dbd82666e800adf30d0249b8ab5

DHA00601972200

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

Mar 19, 2009

Mar 19, 2029