Taiwan FDA registration 961d14691de376e9ac3b72d70c24806d
“GE” Central Monitor Information System
TW: “奇異” 中央監視器資訊系統
Taiwan·Risk Class 2·MD·GE MEDICAL SYSTEMS INFORMATION TECHNOLOGIES·Registered May 22, 2017 – May 22, 2022ExpiredRegistration details
- Analysis ID
- 961d14691de376e9ac3b72d70c24806d
- License Form
- Ministry of Health Medical Device Import No. 029768
- Customs Code
- DHA05602976807
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 devices
- Product Type (Level 2)
- E1025 Arrhythmia detector and alert
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- May 22, 2017
- Expiry Date
- May 22, 2022
About this record
Access comprehensive regulatory information for “GE” Central Monitor Information System in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 961d14691de376e9ac3b72d70c24806d and manufactured by GE MEDICAL SYSTEMS INFORMATION TECHNOLOGIES. The authorized representative in Taiwan is GE MEDICAL SYSTEMS TAIWAN, LTD..
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