"Liko" non-AC-powered patient lift (Non-Sterile)
Taiwan·Risk Class 1·MD·LIKO AB·Registered Sep 07, 2015 – Sep 07, 2020Cancelled- Analysis ID
- 07bfd7aab6ae2dd0f119b95b8a6c9aa5
- License Form
- Ministry of Health Medical Device Import No. 015647
- Customs Code
- DHA09401564702
- Manufacturer
- LIKO AB
- Manufacturer Country
- Sweden
- Authorized Representative
- SHIN FARNG CO., LTD.
- 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
- Registration Date
- Sep 07, 2015
- Expiry Date
- Sep 07, 2020
- Cancellation Date
- Jun 22, 2022
- Status
- Logged out
- Reason
- 許可證已逾有效期
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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.