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SKED Manual patient transfer device(Non-Sterile) - Taiwan Registration 83a15e9b392fa9db9e95ce33cf0347a6

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 83a15e9b392fa9db9e95ce33cf0347a6 and manufactured by SKEDCO, INC.. The authorized representative in Taiwan is ADEPT GENERAL CORP..

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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83a15e9b392fa9db9e95ce33cf0347a6
Registration Details
Taiwan FDA Registration: 83a15e9b392fa9db9e95ce33cf0347a6
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Device Details

SKED Manual patient transfer device(Non-Sterile)
TW: "ๆ€ๅ‡ฑๅพ—"ๆ‰‹ๅ‹•็—…ๆ‚ฃ่ผธ้€่ฃ็ฝฎ(ๆœชๆป…่Œ)
Risk Class 1
MD

Registration Details

83a15e9b392fa9db9e95ce33cf0347a6

Ministry of Health Medical Device Import Registration No. 003597

DHA08400359701

Company Information

United States

Product Details

Limited to the first level of identification scope of the Measures for the Administration of Medical Devices "Manual Patient Transport Device (J.6785)".

J General hospital and personal use equipment

J6785 Manual Patient Conveyor

Imported from abroad

Dates and Status

Oct 01, 2021

Oct 31, 2026