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"Philips" ultrasonic system - Taiwan Registration 0b3a52e1b99a936ba5138f3076ed9aaf

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 0b3a52e1b99a936ba5138f3076ed9aaf and manufactured by Philips Healthcare (Suzhou) Co., Ltd;; 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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0b3a52e1b99a936ba5138f3076ed9aaf
Registration Details
Taiwan FDA Registration: 0b3a52e1b99a936ba5138f3076ed9aaf
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Device Details

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

Registration Details

0b3a52e1b99a936ba5138f3076ed9aaf

DHA09200081808

Company Information

Product Details

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

P Radiology Science

P.1560 ่ถ…้Ÿณๆณขๅ›ž้Ÿณๅฝฑๅƒ็ณป็ตฑ

Input;; Chinese goods;; The use of this device shall comply with the provisions of the Administrative Measures for the Implementation or Use of Medical Devices for Specific Medical Technology Inspection and Testing.

Dates and Status

Mar 07, 2017

Oct 18, 2028