Taiwan FDA registration 12dc92ed309ce32f8b16b5ed106ae81d
"Indeku" Anfei hearing aid analysis system and its accessories
TW: “英德庫”安飛助聽器分析系統及其附件
Taiwan·Risk Class 2·INTERACOUSTICS A/S·Registered Jul 25, 2020 – Jul 25, 2025ExpiredRegistration details
- Analysis ID
- 12dc92ed309ce32f8b16b5ed106ae81d
- Customs Code
- DHA05603381505
Company information
- Manufacturer
- INTERACOUSTICS A/S
- Manufacturer Country
- Denmark
- Authorized Representative
- CLINICO INC.
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.1050 聽力檢查計;; G.3310 助聽器校正器及分析系統
- Import Information
- import
Dates and status
- Registration Date
- Jul 25, 2020
- Expiry Date
- Jul 25, 2025
About this record
Access comprehensive regulatory information for "Indeku" Anfei hearing aid analysis system and its accessories in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 12dc92ed309ce32f8b16b5ed106ae81d and manufactured by INTERACOUSTICS A/S. The authorized representative in Taiwan is CLINICO INC..
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