Taiwan FDA registration d166e50c0bd660f126d22291f48b8cb4
"SKEDCO" Manual patient transfer device (Non-Sterile)
TW: "思開德寇" 手動病患輸送裝置（未滅菌）
Taiwan·Risk Class 1·MD·SKEDCO,INC·Registered Feb 12, 2015 – Feb 12, 2020CancelledRegistration details
- Analysis ID
- d166e50c0bd660f126d22291f48b8cb4
- License Form
- Ministry of Health Medical Device Import No. 014922
- Customs Code
- DHA09401492206
Company information
- Manufacturer
- SKEDCO,INC
- Manufacturer Country
- United States
- Authorized Representative
- REPUTATION AND PROSPERITY CO., LTD.
Product details
- Product Type (Level 1)
- J General hospital and personal use equipment
- Product Type (Level 2)
- J6785 Manual Patient Conveyor
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Feb 12, 2015
- Expiry Date
- Feb 12, 2020
- Cancellation Date
- Aug 05, 2022
Cancellation information
- Status
- Logged out
- Reason
- 未展延而逾期者
About this record
Access comprehensive regulatory information for "SKEDCO" Manual patient transfer device (Non-Sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number d166e50c0bd660f126d22291f48b8cb4 and manufactured by SKEDCO,INC. The authorized representative in Taiwan is REPUTATION AND PROSPERITY CO., LTD..
This page provides complete technical specifications, regulatory compliance details. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.
Free DatabasePowered by Pure Global AI89,000+ Devices