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"ARJO" Patient Lifting (Non-Sterile) - Taiwan Registration f589f62faad191204aa98457cc1e09ca

Access comprehensive regulatory information for "ARJO" Patient Lifting (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 f589f62faad191204aa98457cc1e09ca and manufactured by ARJOHUNTLEIGH POLSKA SP. ZO. O.. The authorized representative in Taiwan is TAIWAN PROFESSIONAL MEDICAL TECHNOLOGY INC..

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f589f62faad191204aa98457cc1e09ca
Registration Details
Taiwan FDA Registration: f589f62faad191204aa98457cc1e09ca
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Device Details

"ARJO" Patient Lifting (Non-Sterile)
TW: "ๆดฑไน…" ็—…ๆ‚ฃ็งปไฝๅ‡้™ๆฉŸ (ๆœชๆป…่Œ)
Risk Class 1
MD

Registration Details

f589f62faad191204aa98457cc1e09ca

Ministry of Health Medical Device Import No. 020311

DHA09402031102

Company Information

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

Apr 15, 2019

Apr 15, 2024