Taiwan FDA registration 3b96fa2e5890b8bf2ee26369bbbbaad0

"Liko" Non-AC-powered patient lift (Non-Sterile)

TW: "立可" 非交流電力式病患升降機 (未滅菌)
Taiwan flagTaiwan·Risk Class 1·MD·LIKO AB·Registered Jun 02, 2020 – Jun 02, 2025Expired
Registration details
Analysis ID
3b96fa2e5890b8bf2ee26369bbbbaad0
License Form
Ministry of Health Medical Device Import No. 021607
Customs Code
DHA09402160702
Company information
Manufacturer
LIKO AB
Manufacturer Country
Sweden
Authorized Representative
Hill-Rom Taiwan Ltd.
Product details
Intended Use
Limited to the first level identification scope of the Measures for the Administration of Medical Equipment "Non-AC Electric Patient Lift (J.5510)".
Product Type (Level 1)
J General hospital and personal use equipment
Product Type (Level 2)
J5510 Non-AC Electric Patient Lift
Import Information
Imported from abroad
Dates and status
Registration Date
Jun 02, 2020
Expiry Date
Jun 02, 2025
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About this record

Access comprehensive regulatory information for "Liko" 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 3b96fa2e5890b8bf2ee26369bbbbaad0 and manufactured by LIKO AB. The authorized representative in Taiwan is Hill-Rom Taiwan Ltd..

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including LIKO AB, and 2 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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