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"KADEN" Wheeled Stretcher (Non-Sterile) - Taiwan Registration 0c7a8ab22b6938c9fae8471c81fe48b5

Access comprehensive regulatory information for "KADEN" Wheeled Stretcher (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 0c7a8ab22b6938c9fae8471c81fe48b5 and manufactured by KADEN INTERNATIONAL LTD.. The authorized representative in Taiwan is PRO-READY ENTERPRISE 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.

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0c7a8ab22b6938c9fae8471c81fe48b5
Registration Details
Taiwan FDA Registration: 0c7a8ab22b6938c9fae8471c81fe48b5
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Device Details

"KADEN" Wheeled Stretcher (Non-Sterile)
TW: "ๅกๅพท"่ผชๅผๆ“”ๅบŠ(ๆœชๆป…่Œ)
Risk Class 1
MD
Cancelled

Registration Details

0c7a8ab22b6938c9fae8471c81fe48b5

Ministry of Health Medical Device Import No. 014122

DHA09401412200

Company Information

Hong Kong

Product Details

J General hospital and personal use equipment

J6910 Wheeled stretcher

Imported from abroad

Dates and Status

May 12, 2014

May 12, 2019

Jun 16, 2022

Cancellation Information

Logged out

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