"Clearear" sound processor - Taiwan Registration d3fa76a31d9cbf24eaadcf35d8a96c77
Access comprehensive regulatory information for "Clearear" sound processor in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number d3fa76a31d9cbf24eaadcf35d8a96c77 and manufactured by COCHLEAR BONE ANCHORED SOLUTIONS AB. The authorized representative in Taiwan is CLINICO INC..
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
For details, it is Chinese approved copy of the imitation order
G ENT Science
G.3300 Hearing Aids
The use of this device shall comply with the provisions of the "Administrative Measures for the Implementation or Use of Medical Devices for Specific Medical Technology Inspection and Testing". input
Dates and Status
Jan 20, 2010
Jan 20, 2025

