Taiwan FDA registration 26935465ee8a6d99813291f5a30e32c9
"Inderku" Leila audiodiagnostic system and its accessories
TW: “英德庫”萊拉聽力診斷系統及其附件
Taiwan·Risk Class 2·INTERACOUSTICS A/S·Registered Jul 30, 2020 – Jul 30, 2025ExpiredRegistration details
- Analysis ID
- 26935465ee8a6d99813291f5a30e32c9
- Customs Code
- DHA05603381801
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)
- K Neuroscience;; G Otolaryngology
- Product Type (Level 2)
- G.1050 聽力檢查計;; K.1900 誘發反應聲刺激器
- Import Information
- import
Dates and status
- Registration Date
- Jul 30, 2020
- Expiry Date
- Jul 30, 2025
About this record
Access comprehensive regulatory information for "Inderku" Leila audiodiagnostic 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 26935465ee8a6d99813291f5a30e32c9 and manufactured by INTERACOUSTICS A/S. 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.
Free DatabasePowered by Pure Global AI89,000+ Devices