Taiwan FDA registration 8d80419d5bf49b54ad962b4affbe2286

"Singular" ultrasound system

TW: "奇異"超音波系統
Taiwan flagTaiwan·Risk Class 2·WIPRO GE HEALTHCARE PVT. LTD.·Registered Jun 16, 2005 – Jun 16, 2020Cancelled
Registration details
Analysis ID
8d80419d5bf49b54ad962b4affbe2286
Customs Code
DHA00601145907
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
Jun 16, 2005
Expiry Date
Jun 16, 2020
Cancellation Date
Jun 22, 2022
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 "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 8d80419d5bf49b54ad962b4affbe2286 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 WIPRO GE HEALTHCARE PVT. LTD., GE VINGMED ULTRASOUND AS, 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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