"SKED" Manual patient transfer device (Non-Sterile)
Taiwan·Risk Class 1·MD·SKEDCO, INC.·Registered Oct 01, 2021 – Oct 31, 2025Expired- Analysis ID
- 89d6325a5218e2234fe2968bf75d5307
- License Form
- Ministry of Health Medical Device Import Registration No. 022039
- Customs Code
- DHA08402203900
- Manufacturer
- SKEDCO, INC.
- Manufacturer Country
- United States
- Authorized Representative
- RAY LONG OUTDOORS CO., LTD.
- 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)
- J6785 Manual Patient Conveyor
- Import Information
- Imported from abroad
- Registration Date
- Oct 01, 2021
- Expiry Date
- Oct 31, 2025
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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 89d6325a5218e2234fe2968bf75d5307 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.