Taiwan FDA registration e27733686738d3b089664dee8bdc80d1
"Cordship" dry laser film (unsterilized)
TW: "康世" 乾式雷射軟片 (未滅菌)
Taiwan·Risk Class 1·CARESTREAM HEALTH, INC.·Registered Jul 06, 2005 – Jul 06, 2020CancelledRegistration details
- Analysis ID
- e27733686738d3b089664dee8bdc80d1
- Customs Code
- DHA04400022402
Company information
- Manufacturer
- CARESTREAM HEALTH, INC.
- Manufacturer Country
- United States
- Authorized Representative
- FAITH BIOMED LTD.
Product details
- Intended Use
- Images can be recorded during diagnostic radiology.
- Product Type (Level 1)
- P Radiology Science
- Product Type (Level 2)
- P.1840 Radiographic film
- Import Information
- import
Dates and status
- Registration Date
- Jul 06, 2005
- Expiry Date
- Jul 06, 2020
- Cancellation Date
- Jun 07, 2022
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Cordship" dry laser film (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number e27733686738d3b089664dee8bdc80d1 and manufactured by CARESTREAM HEALTH, INC.. The authorized representative in Taiwan is FAITH BIOMED LTD..
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