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“ARJO” Patient Lifting (Non-Sterile) - Taiwan Registration 055cf84ca32967d09bbd203382330fd1

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 055cf84ca32967d09bbd203382330fd1 and manufactured by ARJOHUNTLEIGH POLSKA SP. ZO. O.. The authorized representative in Taiwan is YI RUEI ENTERPRISE CO., LTD..

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including ARJO INTERNATIONAL AB, and 1 recent registrations in the same category. 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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055cf84ca32967d09bbd203382330fd1
Registration Details
Taiwan FDA Registration: 055cf84ca32967d09bbd203382330fd1
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Device Details

“ARJO” Patient Lifting (Non-Sterile)
TW: "爾久" 病患移位升降機(未滅菌)
Risk Class 1
MD

Registration Details

055cf84ca32967d09bbd203382330fd1

Ministry of Health Medical Device Import No. 018241

DHA09401824102

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

Aug 28, 2017

Aug 28, 2022

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