Taiwan FDA registration 57daaf692f4ee790f6d2963509846da1

"Singular" ultrasound system

TW: “奇異”超音波系統
Taiwan flagTaiwan·Risk Class 2·WIPRO GE HEALTHCARE PVT. LTD.·Registered Feb 26, 2011 – Feb 26, 2021Cancelled
Registration details
Analysis ID
57daaf692f4ee790f6d2963509846da1
Customs Code
DHA00602207401
Company information
Manufacturer Country
India
Authorized Representative
GE MEDICAL SYSTEMS TAIWAN, LTD.
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.1550 Ultrasonic pulsating Duppler imaging system
Import Information
import
Dates and status
Registration Date
Feb 26, 2011
Expiry Date
Feb 26, 2021
Cancellation Date
Sep 23, 2023
Cancellation information
Status
Logged out
Reason
自行鍵入
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About this record

Access comprehensive regulatory information for "Singular" ultrasound system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 57daaf692f4ee790f6d2963509846da1 and manufactured by WIPRO GE HEALTHCARE PVT. LTD.. The authorized representative in Taiwan is GE MEDICAL SYSTEMS TAIWAN, LTD..

This page provides complete technical specifications, regulatory compliance details, 5 companies making similar products including GE VINGMED ULTRASOUND AS, GE Medical Systems Israel Ltd., 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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