Taiwan FDA registration ccb59a24175576c7ede3d9e8bff70ff3
“GE” Ventilator System
TW: “奇異”呼吸系統
Taiwan·Risk Class 2·MD·DATEX-OHMEDA INC.·Registered Aug 14, 2015 – Aug 14, 2025ExpiredRegistration details
- Analysis ID
- ccb59a24175576c7ede3d9e8bff70ff3
- License Form
- Ministry of Health Medical Device Import No. 027593
- Customs Code
- DHA05602759301
Company information
- Manufacturer
- DATEX-OHMEDA INC.
- 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)
- D Devices for anesthesiology
- Product Type (Level 2)
- D5895 Continuous breathing apparatus
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Aug 14, 2015
- Expiry Date
- Aug 14, 2025
About this record
Access comprehensive regulatory information for “GE” Ventilator System in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number ccb59a24175576c7ede3d9e8bff70ff3 and manufactured by DATEX-OHMEDA INC.. The authorized representative in Taiwan is GE MEDICAL SYSTEMS TAIWAN, LTD..
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