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"Guldmann" Non-AC-powered patient lift (Non-Sterile) - Taiwan Registration 6f49722335a88f52049ff5b2b876001b

Access comprehensive regulatory information for "Guldmann" Non-AC-powered 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 6f49722335a88f52049ff5b2b876001b and manufactured by V. GULDMANN A/S. The authorized representative in Taiwan is EZ-Care Solution Co., Ltd..

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6f49722335a88f52049ff5b2b876001b
Registration Details
Taiwan FDA Registration: 6f49722335a88f52049ff5b2b876001b
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Device Details

"Guldmann" Non-AC-powered patient lift (Non-Sterile)
TW: "้กงๅพทๅ€‘" ้žไบคๆต้›ปๅŠ›ๅผ็—…ๆ‚ฃๅ‡้™ๆฉŸ (ๆœชๆป…่Œ)
Risk Class 1
MD

Registration Details

6f49722335a88f52049ff5b2b876001b

Ministry of Health Medical Device Import No. 013486

DHA09401348607

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

Oct 09, 2013

Oct 09, 2023