“ARJO” Patient Lifting (Non-Sterile) - Taiwan Registration 055cf84ca32967d09bbd203382330fd1
Access comprehensive regulatory information for “ARJO” Patient Lifting (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 055cf84ca32967d09bbd203382330fd1 and manufactured by ARJOHUNTLEIGH POLSKA SP. ZO. O.. The authorized representative in Taiwan is YI RUEI ENTERPRISE CO., LTD..
This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including ARJO INTERNATIONAL AB, and 1 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.
Device Details
Registration Details
055cf84ca32967d09bbd203382330fd1
Ministry of Health Medical Device Import No. 018241
DHA09401824102
Product Details
Limited to the first level identification scope of the Measures for the Administration of Medical Equipment "Non-AC Electric Patient Lift (J.5510)".
J General hospital and personal use equipment
J5510 Non-AC Electric Patient Lift
Imported from abroad
Dates and Status
Aug 28, 2017
Aug 28, 2022

