Taiwan FDA registration b21b4349311cd2789b25079b1b7e7a99
“GE” Holter ECG Analysis Software
TW: “奇異”動態心電圖分析軟體
Taiwan·Risk Class 2·MD·GETEMED Medizin-und Informationstechnik AG·Registered Nov 24, 2017 – Nov 24, 2027ActiveRegistration details
- Analysis ID
- b21b4349311cd2789b25079b1b7e7a99
- License Form
- Ministry of Health Medical Device Import No. 030442
- Customs Code
- DHA05603044203
Company information
- Manufacturer
- GETEMED Medizin-und Informationstechnik AG
- Manufacturer Country
- Germany
- 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)
- E1425 Programmable diagnostic PC
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Nov 24, 2017
- Expiry Date
- Nov 24, 2027
About this record
Access comprehensive regulatory information for “GE” Holter ECG Analysis Software in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number b21b4349311cd2789b25079b1b7e7a99 and manufactured by GETEMED Medizin-und Informationstechnik AG. The authorized representative in Taiwan is GE MEDICAL SYSTEMS TAIWAN, LTD..
This page provides complete technical specifications, regulatory compliance details. 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.
Free DatabasePowered by Pure Global AI89,000+ Devices