Taiwan FDA registration e4a14e51759c292d35437d44807e8f9b
“Carestream” Computed Radiography Equipment
TW: “康世”移動型電腦化放射影像閱讀系統
Taiwan·Risk Class 2·MD·Carestream Health, Ltd.·Registered Mar 31, 2015 – Mar 31, 2020CancelledRegistration details
- Analysis ID
- e4a14e51759c292d35437d44807e8f9b
- License Form
- Ministry of Health Medical Device Import No. 027246
- Customs Code
- DHA05602724606
Company information
- Manufacturer
- Carestream Health, Ltd.
- Manufacturer Country
- Israel
- Authorized Representative
- Taiwan Kangshi Medical Equipment Co., Ltd
Product details
- 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
- Mar 31, 2015
- Expiry Date
- Mar 31, 2020
- Cancellation Date
- Jul 10, 2019
Cancellation information
- Status
- Logged out
- Reason
- 公司歇業
About this record
Access comprehensive regulatory information for “Carestream” Computed Radiography Equipment in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number e4a14e51759c292d35437d44807e8f9b and manufactured by Carestream Health, Ltd.. The authorized representative in Taiwan is Taiwan Kangshi Medical Equipment Co., Ltd.
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