Taiwan FDA registration 00cf06fe83f00615172b67c193f1d871
"SKADE" manual patient transport device (unsterilized)
TW: “斯凱德”手動病患輸送裝置（未滅菌）
Taiwan·Risk Class 1·SKEDCO, INC·Registered Aug 23, 2010 – Aug 23, 2020CancelledRegistration details
- Analysis ID
- 00cf06fe83f00615172b67c193f1d871
- Customs Code
- DHA04400912302
Company information
- Manufacturer
- SKEDCO, INC
- Manufacturer Country
- United States
- Authorized Representative
- FU SHING MEDICAL CO., LTD.
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
- Aug 23, 2010
- Expiry Date
- Aug 23, 2020
- Cancellation Date
- Jun 16, 2022
Cancellation information
- Status
- Logged out
- Reason
- 自行鍵入
About this record
Access comprehensive regulatory information for "SKADE" 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 00cf06fe83f00615172b67c193f1d871 and manufactured by SKEDCO, INC. The authorized representative in Taiwan is FU SHING MEDICAL CO., LTD..
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