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"Philips" ultrasonic system - Taiwan Registration 3a1e9b3ea83f96e594aa68050591f3e8

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 3a1e9b3ea83f96e594aa68050591f3e8 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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3a1e9b3ea83f96e594aa68050591f3e8
Registration Details
Taiwan FDA Registration: 3a1e9b3ea83f96e594aa68050591f3e8
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Device Details

"Philips" ultrasonic system
TW: "้ฃ›ๅˆฉๆตฆ" ่ถ…้Ÿณๆณข็ณป็ตฑ
Risk Class 2

Registration Details

3a1e9b3ea83f96e594aa68050591f3e8

DHA00601149001

Company Information

United States

Product Details

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

P Radiology Science

import

Dates and Status

Jun 29, 2005

Jun 29, 2025