"Kaneta" Manual patient transfer device (Non-Sterile) - Taiwan Registration 31f1c88cd1282b9cc476d45e4bb50a8f
Access comprehensive regulatory information for "Kaneta" 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 31f1c88cd1282b9cc476d45e4bb50a8f and manufactured by KANETA CORPORATION INC.. The authorized representative in Taiwan is ABILITIES HEALTHCARE INCORPORATED.
This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including KANETA CORPORATION INC., 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
31f1c88cd1282b9cc476d45e4bb50a8f
Ministry of Health Medical Device Import Registration No. 018317
DHA08401831700
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, 2023

