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"ARJO" Patient Lift (Non-Sterile) - Taiwan Registration 5b0d1f2fb74b08df0b21cb675c17edbf

Access comprehensive regulatory information for "ARJO" 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 5b0d1f2fb74b08df0b21cb675c17edbf and manufactured by ARJOHUNTLEIGH SINGAPORE PTS LTD.. The authorized representative in Taiwan is ABILITIES HEALTHCARE INCORPORATED.

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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5b0d1f2fb74b08df0b21cb675c17edbf
Registration Details
Taiwan FDA Registration: 5b0d1f2fb74b08df0b21cb675c17edbf
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Device Details

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

Registration Details

5b0d1f2fb74b08df0b21cb675c17edbf

Ministry of Health Medical Device Import No. 013920

DHA09401392000

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

Mar 07, 2014

Mar 07, 2024