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"Guldmann" Patient Lift (Non-Sterile) - Taiwan Registration a6b42f038b46dc7ef4f53931d3db8076

Access comprehensive regulatory information for "Guldmann" Patient Lift (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 a6b42f038b46dc7ef4f53931d3db8076 and manufactured by V. GULDMANN A/S. The authorized representative in Taiwan is ABILITIES HEALTHCARE INCORPORATED.

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a6b42f038b46dc7ef4f53931d3db8076
Registration Details
Taiwan FDA Registration: a6b42f038b46dc7ef4f53931d3db8076
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Device Details

"Guldmann" Patient Lift (Non-Sterile)
TW: "ๅคๆ›ผ" ็—…ๆ‚ฃ็งปไฝๅ‡้™ๆฉŸ (ๆœชๆป…่Œ)
Risk Class 1
MD

Registration Details

a6b42f038b46dc7ef4f53931d3db8076

Ministry of Health Medical Device Import No. 013922

DHA09401392201

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

J5510 Non-AC Electric Patient Lift

Imported from abroad

Dates and Status

Mar 07, 2014

Mar 07, 2024