Taiwan FDA registration 164051ad51e8b37a40aef7659b92bb77

"Philips" ultrasonic system

TW: “飛利浦”超音波系統
Taiwan flagTaiwan·Risk Class 2·PHILIPS ULTRASOUND, INC.·Registered Jul 20, 2012 – Jul 20, 2017Cancelled
Registration details
Analysis ID
164051ad51e8b37a40aef7659b92bb77
Customs Code
DHA00602390201
Company information
Manufacturer Country
United States
Authorized Representative
PHILIPS TAIWAN LIMITED
Product details
Intended Use
For details, it is Chinese approved copy of the imitation order
Product Type (Level 1)
P Radiology Science
Product Type (Level 2)
P.1560 Ultrasonic Echo Imaging System;; P.1570 Ultrasound converters for diagnostic use;; P.1550 Ultrasonic pulsating Duppler imaging system
Import Information
import
Dates and status
Registration Date
Jul 20, 2012
Expiry Date
Jul 20, 2017
Cancellation Date
Dec 13, 2019
Cancellation information
Status
Logged out
Reason
許可證已逾有效期
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About this record

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 164051ad51e8b37a40aef7659b92bb77 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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