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"Goodman" patient lift (unsterilized) - Taiwan Registration 5f9b2ee0e5957edc60f006d934146cc1

Access comprehensive regulatory information for "Goodman" patient lift (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 5f9b2ee0e5957edc60f006d934146cc1 and manufactured by V. GULDMANN A/S. The authorized representative in Taiwan is FUROTO MEDICAL & WELFARE 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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5f9b2ee0e5957edc60f006d934146cc1
Registration Details
Taiwan FDA Registration: 5f9b2ee0e5957edc60f006d934146cc1
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Device Details

"Goodman" patient lift (unsterilized)
TW: โ€œๅคๅพทๆ›ผโ€็—…ๆ‚ฃ็งปไฝๅ‡้™ๆฉŸ(ๆœชๆป…่Œ)
Risk Class 1
Cancelled

Registration Details

5f9b2ee0e5957edc60f006d934146cc1

DHA04400608008

Company Information

Denmark

Product Details

Limited to the first level identification scope of the Measures for the Administration of Medical Equipment "Non-AC Electric Patient Lift (J.5510)".

J General hospital and personal use equipment

J.5510 Non-AC electric patient lifts

import

Dates and Status

Aug 10, 2007

Aug 10, 2017

Nov 26, 2019

Cancellation Information

Logged out

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