Manufacturer profileSKEDCO,INC
TaiwanUnited States3 products registeredFeb 12, 2015 – Oct 01, 2021
VerifiedTFDA · Taiwan Food and Drug Administration registry
3
Total products
2
Product types
1
Active products
Oct 2021
Latest registration
Company details
- Address
- P.O.BOX 3390 10505 SW MANHASSET DRIVE, TUALATIN, OREGON 97062 USA
Regulatory footprint
Search SKEDCO,INC across other regulatory registries
Thailand
European Union
Colombia
South Korea
Canada
EcuadorRecent registrations
Latest 5 products registered by this manufacturer
Most popular products
Products with most registrations
Authorized representatives
Taiwan authorized representatives for this manufacturer
Recent registered products
Most recent products (showing top 20)
"SKED" Manual patient transfer device (Non-Sterile)
Registered: Oct 01, 2021 • Expires: Oct 31, 2025
- Risk Class
- Class 1
- Type
- MD
- AR
- REPUTATION AND PROSPERITY CO., LTD.
"SKED" Manual patient transfer device (Non-Sterile)
Registered: Apr 08, 2020 • Expires: Apr 08, 2025
Cancelled
- Risk Class
- Class 1
- Type
- MD
- AR
- REPUTATION AND PROSPERITY CO., LTD.
"SKEDCO" Manual patient transfer device (Non-Sterile)
Registered: Feb 12, 2015 • Expires: Feb 12, 2020
Cancelled
- Risk Class
- Class 1
- Type
- MD
- AR
- REPUTATION AND PROSPERITY CO., LTD.
About this profile
Explore comprehensive manufacturer profile for SKEDCO,INC based in United States through Pure Global AI's free Taiwan medical device database. This manufacturer has 3 products registered in Taiwan across 2 unique product categories. Their regulatory history spans from Feb 12, 2015 to Oct 01, 2021.
This page provides detailed insights including 3 recent product registrations, 2 most popular products with "SKED" Manual patient transfer device (Non-Sterile) having 2 registrations, and 1 authorized representatives including REPUTATION AND PROSPERITY CO., LTD.. Pure Global AI offers free access to Taiwan's medical device database, enabling global MedTech companies to analyze market dynamics and identify opportunities.