Taiwan FDA registration 3f7e425123df94a64ef11525837738d9

"Singular" patient monitor

TW: “奇異”病患監視器
Taiwan flagTaiwan·Risk Class 2·GE HEALTHCARE FINLAND OY·Registered Nov 01, 2011 – Nov 01, 2026Active
Registration details
Analysis ID
3f7e425123df94a64ef11525837738d9
Customs Code
DHA00602291301
Company information
Manufacturer Country
Finland
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)
E Cardiovascular Medicine Science
Product Type (Level 2)
E.2300 Cardiac monitor (including cardiac data and heart rate monitor)
Import Information
import
Dates and status
Registration Date
Nov 01, 2011
Expiry Date
Nov 01, 2026
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About this record

Access comprehensive regulatory information for "Singular" patient monitor in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 3f7e425123df94a64ef11525837738d9 and manufactured by GE HEALTHCARE FINLAND OY. 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 Critikon De Mexico S. De R.L. De C.V., 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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