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"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.

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31f1c88cd1282b9cc476d45e4bb50a8f
Registration Details
Taiwan FDA Registration: 31f1c88cd1282b9cc476d45e4bb50a8f
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Device Details

"Kaneta" Manual patient transfer device (Non-Sterile)
TW: "่‚ฏ่ธ" ๆ‰‹ๅ‹•็—…ๆ‚ฃ่ผธ้€่ฃ็ฝฎ (ๆœชๆป…่Œ)
Risk Class 1
MD

Registration Details

31f1c88cd1282b9cc476d45e4bb50a8f

Ministry of Health Medical Device Import Registration No. 018317

DHA08401831700

Company Information

Japan

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

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