Taiwan FDA registration 0c5b2173ec197f647e347060dbb3d76c

"Singular" X-ray machine autoclave generator for diagnostics (unsterilized)

TW: "奇異" 診斷用X光機高壓產生器(未滅菌)
Taiwan flagTaiwan·Risk Class 1·WIPRO GE HEALTHCARE PRIVATE LTD.·Registered Oct 01, 2021 – Oct 31, 2025Expired
Registration details
Analysis ID
0c5b2173ec197f647e347060dbb3d76c
Customs Code
DHA08402067900
Company information
Manufacturer Country
India
Authorized Representative
GE MEDICAL SYSTEMS TAIWAN, LTD.
Product details
Intended Use
Limited to the first level identification range of the classification and grading management measures for medical equipment "high-pressure generator for diagnostic X-ray machine (P.1700)".
Product Type (Level 1)
P Radiology Science
Product Type (Level 2)
P.1700 診斷用X光機高壓產生器
Import Information
QMS/QSD;; Input;; Consent letter must be attached to the import (consent from the Atomic Energy Commission must be obtained for each import)
Dates and status
Registration Date
Oct 01, 2021
Expiry Date
Oct 31, 2025
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About this record

Access comprehensive regulatory information for "Singular" X-ray machine autoclave generator for diagnostics (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 0c5b2173ec197f647e347060dbb3d76c and manufactured by WIPRO GE HEALTHCARE PRIVATE LTD.. The authorized representative in Taiwan is GE MEDICAL SYSTEMS TAIWAN, LTD..

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including WIPRO GE HEALTHCARE PRIVATE LTD., and 1 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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