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"WyEast" TOTALIFT (Non-Sterile) - Taiwan Registration 291b9d56c83d9368452d50682fb536eb

Access comprehensive regulatory information for "WyEast" TOTALIFT (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 291b9d56c83d9368452d50682fb536eb and manufactured by WYEAST MEDICAL CORPORATION. The authorized representative in Taiwan is PROMEDICAL 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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291b9d56c83d9368452d50682fb536eb
Registration Details
Taiwan FDA Registration: 291b9d56c83d9368452d50682fb536eb
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Device Details

"WyEast" TOTALIFT (Non-Sterile)
TW: "่ก›ๆ˜“" ๆฐดๅนณ่ผธ้€ๆฌ้‹่ฃ็ฝฎ (ๆœชๆป…่Œ)
Risk Class 1
MD
Cancelled

Registration Details

291b9d56c83d9368452d50682fb536eb

Ministry of Health Medical Device Import No. 014898

DHA09401489809

Company Information

United States

Product Details

J General hospital and personal use equipment

J6785 Manual Patient Conveyor

Imported from abroad

Dates and Status

Feb 03, 2015

Feb 03, 2020

Aug 05, 2022

Cancellation Information

Logged out

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