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"Liko" non-AC-powered patient lift (Non-Sterile) - Taiwan Registration 07bfd7aab6ae2dd0f119b95b8a6c9aa5

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 07bfd7aab6ae2dd0f119b95b8a6c9aa5 and manufactured by LIKO AB. The authorized representative in Taiwan is SHIN FARNG CO., 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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07bfd7aab6ae2dd0f119b95b8a6c9aa5
Registration Details
Taiwan FDA Registration: 07bfd7aab6ae2dd0f119b95b8a6c9aa5
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Device Details

"Liko" non-AC-powered patient lift (Non-Sterile)
TW: "ๅˆฉๅฏ" ้žไบคๆต้›ปๅŠ›ๅผ็—…ๆ‚ฃๅ‡้™ๆฉŸ (ๆœชๆป…่Œ)
Risk Class 1
MD
Cancelled

Registration Details

07bfd7aab6ae2dd0f119b95b8a6c9aa5

Ministry of Health Medical Device Import No. 015647

DHA09401564702

Company Information

Sweden

Product Details

J General hospital and personal use equipment

J5510 Non-AC Electric Patient Lift

Imported from abroad

Dates and Status

Sep 07, 2015

Sep 07, 2020

Jun 22, 2022

Cancellation Information

Logged out

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