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"Kaneta" Manual patient transfer device (Non-Sterile) - Taiwan Registration 4a02358f0c0b24c0b9a306b0407fcbd8

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 4a02358f0c0b24c0b9a306b0407fcbd8 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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4a02358f0c0b24c0b9a306b0407fcbd8
Registration Details
Taiwan FDA Registration: 4a02358f0c0b24c0b9a306b0407fcbd8
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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
Cancelled

Registration Details

4a02358f0c0b24c0b9a306b0407fcbd8

Ministry of Health Medical Device Import No. 018317

DHA09401831709

Company Information

Japan

Product Details

J General hospital and personal use equipment

J6785 Manual Patient Conveyor

Imported from abroad

Dates and Status

Sep 18, 2017

Sep 18, 2022

Cancellation Information

Logged out

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