Reanda Non-AC Electric Patient Lift (Unsterilized) - Taiwan Registration 9483375422be272baae5047003b60849
Access comprehensive regulatory information for Reanda Non-AC Electric Patient Lift (Unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 9483375422be272baae5047003b60849 and manufactured by SUZHOU IRELAND MEDICAL EQUIPMENT CO., LTD. The authorized representative in Taiwan is PROMEDICAL CO., 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.
Device Details
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
J.5510 Non-AC electric patient lifts
Input;; Chinese goods
Dates and Status
Apr 27, 2021
Apr 27, 2026
Sep 15, 2022
Cancellation Information
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