"ARJO" Patient Lifting (Non-Sterile) - Taiwan Registration f589f62faad191204aa98457cc1e09ca
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 f589f62faad191204aa98457cc1e09ca and manufactured by ARJOHUNTLEIGH POLSKA SP. ZO. O.. The authorized representative in Taiwan is TAIWAN PROFESSIONAL MEDICAL TECHNOLOGY INC..
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.
Device Details
Registration Details
f589f62faad191204aa98457cc1e09ca
Ministry of Health Medical Device Import No. 020311
DHA09402031102
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
Apr 15, 2019
Apr 15, 2024

