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Taiwan FDA registration 9f2e68b67ec71bc0e139cc6c05e4eaea

"Singular" pulse oximeter module

TW: "奇異" 脈搏血氧儀模組
Taiwan flagTaiwan·Risk Class 2·GE MEDICAL SYSTEMS INFORMATION TECHNOLOGIES·Registered Oct 03, 2005 – Oct 03, 2015Cancelled
Registration details
Analysis ID
9f2e68b67ec71bc0e139cc6c05e4eaea
Customs Code
DHA00601258606
Company information
Manufacturer
GE MEDICAL SYSTEMS INFORMATION TECHNOLOGIES
Manufacturer Country
United States
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.2700.
Import Information
import
Dates and status
Registration Date
Oct 03, 2005
Expiry Date
Oct 03, 2015
Cancellation Date
Apr 25, 2018
Cancellation information
Status
Logged out
Reason
自行鍵入
About this record

Access comprehensive regulatory information for "Singular" pulse oximeter module in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 9f2e68b67ec71bc0e139cc6c05e4eaea and manufactured by GE MEDICAL SYSTEMS INFORMATION TECHNOLOGIES. The authorized representative in Taiwan is GE MEDICAL SYSTEMS TAIWAN, LTD..

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