Taiwan FDA registration 4fad5c8567f80939b52605b7904aa441
"Skytec" manual patient transport device (unsterilized)
TW: "思凱得"手動病患輸送裝置(未滅菌)
Taiwan·Risk Class 1·SKEDCO, INC.·Registered Apr 12, 2006 – Apr 12, 2026CancelledRegistration details
- Analysis ID
- 4fad5c8567f80939b52605b7904aa441
- Customs Code
- DHA04400359704
Company information
- Manufacturer
- SKEDCO, INC.
- Manufacturer Country
- United States
- Authorized Representative
- ADEPT GENERAL CORP.
Product details
- Intended Use
- Limited to the first level of identification scope of the Measures for the Administration of Medical Devices "Manual Patient Transport Device (J.6785)".
- Product Type (Level 1)
- J General hospital and personal use equipment
- Product Type (Level 2)
- J.6785 Manual Patient Conveying Device
- Import Information
- import
Dates and status
- Registration Date
- Apr 12, 2006
- Expiry Date
- Apr 12, 2026
- Cancellation Date
- Sep 30, 2021
Cancellation information
- Status
- Logged out
- Reason
- 轉為登錄字號
About this record
Access comprehensive regulatory information for "Skytec" manual patient transport device (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 4fad5c8567f80939b52605b7904aa441 and manufactured by SKEDCO, INC.. The authorized representative in Taiwan is ADEPT GENERAL CORP..
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