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“MED-EL” Mi1000 CONCERTO Cochlear Implant - Taiwan Registration 9e2dec725847e9b4e5df7befc2862c2c

Access comprehensive regulatory information for “MED-EL” Mi1000 CONCERTO Cochlear Implant in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number 9e2dec725847e9b4e5df7befc2862c2c and manufactured by MED-EL ELEKTROMEDIZINISCHE GERAETE GMBH. The authorized representative in Taiwan is MELODY MEDICAL INSTRUMENTS CORPORATION.

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.

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9e2dec725847e9b4e5df7befc2862c2c
Registration Details
Taiwan FDA Registration: 9e2dec725847e9b4e5df7befc2862c2c
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Device Details

“MED-EL” Mi1000 CONCERTO Cochlear Implant
TW: “美樂迪”人工電子耳
Risk Class 3
MD

Registration Details

9e2dec725847e9b4e5df7befc2862c2c

Department of Health Medical Device Import No. 023258

DHA00602325800

Company Information

Product Details

For details, it is Chinese approved copy of the imitation order

G ENT device

G0001 Cochlear implant

Imported from abroad; The use of this equipment shall comply with the "Administrative Measures for the Implementation or Use of Specific Medical Technical Examination and Inspection Medical Equipment"

Dates and Status

Feb 17, 2012

Feb 17, 2027