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"Dayi" non-AC electric patient lift bed (unsterilized) - Taiwan Registration e55b24cd75f0fd9f8504d9f701e9fb27

Access comprehensive regulatory information for "Dayi" non-AC electric patient lift bed (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number e55b24cd75f0fd9f8504d9f701e9fb27 and manufactured by Dayi Medical Instrument Factory. The authorized representative in Taiwan is Dayi Medical Instrument Factory.

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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e55b24cd75f0fd9f8504d9f701e9fb27
Registration Details
Taiwan FDA Registration: e55b24cd75f0fd9f8504d9f701e9fb27
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Device Details

"Dayi" non-AC electric patient lift bed (unsterilized)
TW: โ€œๅคงๅ„„โ€้žไบคๆต้›ปๅ‹•็—…ๆ‚ฃ็งปไฝๅบŠ (ๆœชๆป…่Œ)
Risk Class 1
Cancelled

Registration Details

e55b24cd75f0fd9f8504d9f701e9fb27

Company Information

Taiwan, Province of China

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

Domestic

Dates and Status

Feb 04, 2009

Feb 04, 2014

Dec 14, 2016

Cancellation Information

Logged out

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