Taiwan FDA registration b63f56bfb6a85886c929a005f8c56d72
"Bizarre" high-output neonatal phototherapy instrument
TW: "奇異"高輸出新生兒光療儀
Taiwan·Risk Class 2·OHMEDA MEDICAL,DIVISION OF DATEX-OHMEDA, INC.·Registered Dec 13, 2005 – Dec 13, 2015CancelledRegistration details
- Analysis ID
- b63f56bfb6a85886c929a005f8c56d72
- Customs Code
- DHA00601380803
Company information
- Manufacturer
- OHMEDA MEDICAL,DIVISION OF 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)
- J General hospital and personal use equipment
- Product Type (Level 2)
- J.5400 新生兒保溫箱
- Import Information
- import
Dates and status
- Registration Date
- Dec 13, 2005
- Expiry Date
- Dec 13, 2015
- Cancellation Date
- Apr 25, 2018
Cancellation information
- Status
- Logged out
- Reason
- 自行鍵入
About this record
Access comprehensive regulatory information for "Bizarre" high-output neonatal phototherapy instrument in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number b63f56bfb6a85886c929a005f8c56d72 and manufactured by OHMEDA MEDICAL,DIVISION OF DATEX-OHMEDA, INC.. The authorized representative in Taiwan is GE MEDICAL SYSTEMS TAIWAN, LTD..
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