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"ROPOX" Non-AC-powered patient lift (Non-Sterile) - Taiwan Registration e7d9260ff9e35f5ab06c65965a935234

Access comprehensive regulatory information for "ROPOX" Non-AC-powered 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 e7d9260ff9e35f5ab06c65965a935234 and manufactured by ROPOX A/S. 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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e7d9260ff9e35f5ab06c65965a935234
Registration Details
Taiwan FDA Registration: e7d9260ff9e35f5ab06c65965a935234
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Device Details

"ROPOX" Non-AC-powered patient lift (Non-Sterile)
TW: "็พ…ๅธ•ๆ–ฏ" ้žไบคๆต้›ปๅŠ›ๅผ็—…ๆ‚ฃๅ‡้™ๆฉŸ (ๆœชๆป…่Œ)
Risk Class 1
MD

Registration Details

e7d9260ff9e35f5ab06c65965a935234

Ministry of Health Medical Device Import No. 021756

DHA09402175606

Company Information

Denmark

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

Jul 20, 2020

Jul 20, 2025