Taiwan FDA registration 46930c9f1aeb643ee0651db02928ff0b
"GE" Definium XR120 Digital X-ray imaging system
TW: "奇異"X光數位偵檢器
Taiwan·Risk Class 2·MD·Rayence Co., Ltd.·Registered Jul 20, 2021 – Jul 20, 2026ExpiredRegistration details
- Analysis ID
- 46930c9f1aeb643ee0651db02928ff0b
- License Form
- Ministry of Health Medical Device Import No. 034764
- Customs Code
- DHA05603476406
Company information
- Manufacturer
- Rayence Co., Ltd.
- Manufacturer Country
- Korea, Republic of
- Authorized Representative
- GE MEDICAL SYSTEMS TAIWAN, LTD.
Product details
- Intended Use
- Details are as detailed as approved Chinese instructions
- Product Type (Level 1)
- P Devices for radiology
- Product Type (Level 2)
- P1650 fluoroscopic X-ray image intensifier
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Jul 20, 2021
- Expiry Date
- Jul 20, 2026
About this record
Access comprehensive regulatory information for "GE" Definium XR120 Digital X-ray imaging system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 46930c9f1aeb643ee0651db02928ff0b and manufactured by Rayence Co., Ltd.. The authorized representative in Taiwan is GE MEDICAL SYSTEMS TAIWAN, LTD..
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