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"SKEDCO" Manual patient transfer device (Non-Sterile) - Taiwan Registration d166e50c0bd660f126d22291f48b8cb4

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.

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d166e50c0bd660f126d22291f48b8cb4
Registration Details
Taiwan FDA Registration: d166e50c0bd660f126d22291f48b8cb4
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Device Details

"SKEDCO" Manual patient transfer device (Non-Sterile)
TW: "ๆ€้–‹ๅพทๅฏ‡" ๆ‰‹ๅ‹•็—…ๆ‚ฃ่ผธ้€่ฃ็ฝฎ๏ผˆๆœชๆป…่Œ๏ผ‰
Risk Class 1
MD
Cancelled

Registration Details

d166e50c0bd660f126d22291f48b8cb4

Ministry of Health Medical Device Import No. 014922

DHA09401492206

Company Information

United States

Product Details

J General hospital and personal use equipment

J6785 Manual Patient Conveyor

Imported from abroad

Dates and Status

Feb 12, 2015

Feb 12, 2020

Aug 05, 2022

Cancellation Information

Logged out

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