Taiwan FDA registration 966befc75173c6c43219a2728d01c104
Lidco non-AC electric patient lift sling (unsterilized)
TW: "立可" 非交流電力式病患升降機用懸吊帶 (未滅菌)
Registration details
- Analysis ID
- 966befc75173c6c43219a2728d01c104
- Customs Code
- DHA09600451302
Company information
- Manufacturer
- SHL Healthcare Ltd.;; LIKO AB
- Manufacturer Country
- Sweden;;China
- Authorized Representative
- Hill-Rom Taiwan Ltd.
Product details
- Intended Use
- Limited to the first level identification scope of the "Non-AC Power Patient Lift (J.5510)" of the Measures for the Classification and Grading Management of Medical Equipment.
- Product Type (Level 1)
- J General hospital and personal use equipment
- Product Type (Level 2)
- J.5510 Non-AC electric patient lifts
- Import Information
- Chinese goods;; Contract manufacturing;; input
Dates and status
- Registration Date
- Apr 28, 2021
- Expiry Date
- Apr 28, 2026
About this record
Access comprehensive regulatory information for Lidco non-AC electric patient lift sling (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 966befc75173c6c43219a2728d01c104 and manufactured by SHL Healthcare Ltd.;; LIKO AB. The authorized representative in Taiwan is Hill-Rom Taiwan Ltd..
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.
Free DatabasePowered by Pure Global AI89,000+ Devices