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"Philips" ultrasonic system - Taiwan Registration 8ce18bcb404c1ed9a330b8db909e90e8

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 8ce18bcb404c1ed9a330b8db909e90e8 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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8ce18bcb404c1ed9a330b8db909e90e8
Registration Details
Taiwan FDA Registration: 8ce18bcb404c1ed9a330b8db909e90e8
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Device Details

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

Registration Details

8ce18bcb404c1ed9a330b8db909e90e8

DHA05602600403

Company Information

United States

Product Details

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

P Radiology Science

P.1560 Ultrasonic Echo Imaging System;; P.1570 Ultrasound converters for diagnostic use;; P.1550 Ultrasonic pulsating Duppler imaging system

import

Dates and Status

Mar 14, 2014

Mar 14, 2024