Taiwan FDA registration 18c53e3a2107aef9ec0ec5dc570be9fb
"Singular" heart electrode Su compounder
TW: "奇異"心臟電極蘇復器
Taiwan·Risk Class 2·GE MEDICAL SYSTEMS INFORMATION TECHNOLOGIES GMBH·Registered Dec 20, 2005 – Dec 20, 2020CancelledRegistration details
- Analysis ID
- 18c53e3a2107aef9ec0ec5dc570be9fb
- Customs Code
- DHA00601382302
Company information
- Manufacturer
- GE MEDICAL SYSTEMS INFORMATION TECHNOLOGIES GMBH
- 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 Medicine Science
- Import Information
- import
Dates and status
- Registration Date
- Dec 20, 2005
- Expiry Date
- Dec 20, 2020
- Cancellation Date
- Jun 22, 2022
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Singular" heart electrode Su compounder in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 18c53e3a2107aef9ec0ec5dc570be9fb and manufactured by GE MEDICAL SYSTEMS INFORMATION TECHNOLOGIES GMBH. The authorized representative in Taiwan is GE MEDICAL SYSTEMS TAIWAN, LTD..
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