"Qinda" sputum collector (sterilized) - Taiwan Registration 162fe01e34ccafdf0e49c39e538656b1
Access comprehensive regulatory information for "Qinda" sputum collector (sterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 162fe01e34ccafdf0e49c39e538656b1 and manufactured by HOSPITECH MANUFACTURING SERVICES SDN BHD. The authorized representative in Taiwan is TEAM POWER MEDICAL INSTRUMENT LTD..
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Device Details
Product Details
Limited to the first level recognition range of the Measures for the Administration of Medical Devices "Vacuum-powered Body Fluid Absorption Devices (J.6740)".
J General hospital and personal use equipment
J.6740 Vacuum-powered fluid absorption apparatus
Input;; QMS/QSD
Dates and Status
Oct 25, 2011
Oct 25, 2021
Sep 23, 2023
Cancellation Information
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