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"Beren" manual patient transport device (unsterilized) - Taiwan Registration 578d84a6bf9c6b10bb51ca6427814e5e

Access comprehensive regulatory information for "Beren" manual patient transport device (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 578d84a6bf9c6b10bb51ca6427814e5e and manufactured by Borun Industrial Co., Ltd. Kaohsiung Factory. The authorized representative in Taiwan is GRAND HEALTHCARE 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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578d84a6bf9c6b10bb51ca6427814e5e
Registration Details
Taiwan FDA Registration: 578d84a6bf9c6b10bb51ca6427814e5e
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Device Details

"Beren" manual patient transport device (unsterilized)
TW: โ€œๆŸๅ€ซโ€ๆ‰‹ๅ‹•็—…ๆ‚ฃ่ผธ้€่ฃ็ฝฎ(ๆœชๆป…่Œ)
Risk Class 1
Cancelled

Registration Details

578d84a6bf9c6b10bb51ca6427814e5e

Company Information

Taiwan, Province of China

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

J.6785 Manual Patient Conveying Device

Domestic

Dates and Status

Aug 08, 2012

Aug 08, 2017

Dec 20, 2019

Cancellation Information

Logged out

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