Taiwan FDA registration 9e2dec725847e9b4e5df7befc2862c2c
“MED-EL” Mi1000 CONCERTO Cochlear Implant
TW: “美樂迪”人工電子耳
Taiwan·Risk Class 3·MD·MED-EL ELEKTROMEDIZINISCHE GERAETE GMBH·Registered Feb 17, 2012 – Feb 17, 2027ActiveRegistration details
- Analysis ID
- 9e2dec725847e9b4e5df7befc2862c2c
- License Form
- Department of Health Medical Device Import No. 023258
- Customs Code
- DHA00602325800
Company information
- Manufacturer
- MED-EL ELEKTROMEDIZINISCHE GERAETE GMBH
- Manufacturer Country
- Austria
- Authorized Representative
- MELODY MEDICAL INSTRUMENTS CORPORATION
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- G ENT device
- Product Type (Level 2)
- G0001 Cochlear implant
- Import Information
- 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
- Registration Date
- Feb 17, 2012
- Expiry Date
- Feb 17, 2027
About this record
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.
Free DatabasePowered by Pure Global AI89,000+ Devices