Taiwan FDA registration aadf7099dd8c593d4fc73166a1ce8e9b
"Merondi" bone guided auditory implant system
TW: “美樂迪”骨導式聽覺植入系統
Taiwan·Risk Class 2·MED-EL Elektromedizinische Geräte GmbH; VIBRANT MED-EL HEARING TECHNOLOGY GMBH·Registered Jan 21, 2014 – Jan 21, 2019CancelledRegistration details
- Analysis ID
- aadf7099dd8c593d4fc73166a1ce8e9b
- Customs Code
- DHA05602534804
Company information
- 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 Science
- Product Type (Level 2)
- G.3300 Hearing Aids
- Import Information
- import
Dates and status
- Registration Date
- Jan 21, 2014
- Expiry Date
- Jan 21, 2019
- Cancellation Date
- Jul 15, 2022
Cancellation information
- Status
- Logged out
- Reason
- 未展延而逾期者
About this record
Access comprehensive regulatory information for "Merondi" bone guided auditory implant system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number aadf7099dd8c593d4fc73166a1ce8e9b and manufactured by MED-EL Elektromedizinische Geräte GmbH; VIBRANT MED-EL HEARING TECHNOLOGY GMBH. The authorized representative in Taiwan is MELODY MEDICAL INSTRUMENTS CORPORATION.
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