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“RoMedic”Patient Lifters (Non-Sterile) - Taiwan Registration 3188eb070fc15406b511b16e1213992e

Access comprehensive regulatory information for “RoMedic”Patient Lifters (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 3188eb070fc15406b511b16e1213992e and manufactured by HANDICARE AB. The authorized representative in Taiwan is THERALIFE INTERVENTION CARE COMPANY LIMITED.

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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3188eb070fc15406b511b16e1213992e
Registration Details
Taiwan FDA Registration: 3188eb070fc15406b511b16e1213992e
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Device Details

“RoMedic”Patient Lifters (Non-Sterile)
TW: “羅麥迪克”病患移位升降機 (未滅菌)
Risk Class 1
MD

Registration Details

3188eb070fc15406b511b16e1213992e

Ministry of Health Medical Device Import No. 020988

DHA09402098809

Company Information

Sweden

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 28, 2019

Oct 28, 2024