Taiwan FDA registration 3fc0afe72bd076377a27f9c800f382f7

"Strange" patient physiology monitor

TW: “奇異”病患生理監視器
Taiwan flagTaiwan·Risk Class 3·BEIJING KEWEI CLINICAL DIAGNOSTIC REAGENT INC.·Registered Nov 02, 2010 – Nov 02, 2015Cancelled
Registration details
Analysis ID
3fc0afe72bd076377a27f9c800f382f7
Customs Code
DHA04200029002
Company information
Manufacturer Country
China
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.1025 Arrhythmia Detectors and Alerts
Import Information
import
Dates and status
Registration Date
Nov 02, 2010
Expiry Date
Nov 02, 2015
Cancellation Date
Apr 25, 2018
Cancellation information
Status
Logged out
Reason
自行鍵入
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About this record

Access comprehensive regulatory information for "Strange" patient physiology monitor in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number 3fc0afe72bd076377a27f9c800f382f7 and manufactured by BEIJING KEWEI CLINICAL DIAGNOSTIC REAGENT INC.. The authorized representative in Taiwan is GE MEDICAL SYSTEMS TAIWAN, LTD..

This page provides complete technical specifications, regulatory compliance details, 3 companies making similar products including GE MEDICAL SYSTEMS INFORMATION TECHNOLOGIES, GE MEDICAL SYSTEMS INFORMATION TECHNOLOGIES, INC., 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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