“TUFFCARE” Non-AC-powered patient lift(Non-sterile) - Taiwan Registration 0a20f4e4a53b9efeb7827cb6500f4c6e
Access comprehensive regulatory information for “TUFFCARE” Non-AC-powered patient lift(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 0a20f4e4a53b9efeb7827cb6500f4c6e and manufactured by SHIN-I MEDICAL MANUFACTURING CO., LTD.. The authorized representative in Taiwan is SHIN-I MEDICAL MANUFACTURING 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.
Device Details
Registration Details
0a20f4e4a53b9efeb7827cb6500f4c6e
Ministry of Health Medical Device Manufacturing No. 008636
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
Produced in Taiwan, China
Dates and Status
Oct 15, 2020
Oct 15, 2025