"SKED" Manual patient transfer device (Non-Sterile)
Taiwan·Risk Class 1·MD·SKEDCO, INC.·Registered Oct 16, 2020 – Oct 16, 2025Cancelled- Analysis ID
- 4aa968f2232a23a10dc3d34a26e8fbc9
- License Form
- Ministry of Health Medical Device Import No. 022039
- Customs Code
- DHA09402203909
- Manufacturer
- SKEDCO, INC.
- Manufacturer Country
- United States
- Authorized Representative
- RAY LONG OUTDOORS CO., LTD.
- Product Type (Level 1)
- J General hospital and personal use equipment
- Product Type (Level 2)
- J6785 Manual Patient Conveyor
- Import Information
- Imported from abroad
- Registration Date
- Oct 16, 2020
- Expiry Date
- Oct 16, 2025
- Status
- Logged out
- Reason
- 轉為登錄字號
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Access comprehensive regulatory information for "SKED" 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 4aa968f2232a23a10dc3d34a26e8fbc9 and manufactured by SKEDCO, INC.. The authorized representative in Taiwan is RAY LONG OUTDOORS CO., LTD..
This page provides complete technical specifications, regulatory compliance details, 2 companies making similar products including SKEDCO,INC, SKEDCO, INC., and 3 recent registrations in the same category. 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.