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“ARJO” Patient Lifting (Non-Sterile) - Taiwan Registration 31863ba4b8dbf9dff64c883ae664e48a

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 31863ba4b8dbf9dff64c883ae664e48a and manufactured by ARJO INTERNATIONAL AB. The authorized representative in Taiwan is TAIWAN PROFESSIONAL MEDICAL TECHNOLOGY INC..

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including ARJOHUNTLEIGH POLSKA SP. ZO. O., 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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31863ba4b8dbf9dff64c883ae664e48a
Registration Details
Taiwan FDA Registration: 31863ba4b8dbf9dff64c883ae664e48a
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Device Details

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

Registration Details

31863ba4b8dbf9dff64c883ae664e48a

Ministry of Health Medical Device Import No. 018272

DHA09401827200

Company Information

Canada

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

Sep 05, 2017

Sep 05, 2022

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