Taiwan FDA registration 6eabc2c89e7633cca01b062a8c6728f0
"Inte Yakusti" Titan handheld system
TW: “音特亞庫斯提”泰坦手持系統
Taiwan·Risk Class 2·INTERACOUSTICS A/S·Registered May 13, 2014 – May 13, 2019CancelledRegistration details
- Analysis ID
- 6eabc2c89e7633cca01b062a8c6728f0
- Customs Code
- DHA05602616402
Company information
- Manufacturer
- INTERACOUSTICS A/S
- Manufacturer Country
- Denmark
- Authorized Representative
- Baiou Precision Co., Ltd
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
- May 13, 2014
- Expiry Date
- May 13, 2019
- Cancellation Date
- Jun 16, 2022
Cancellation information
- Status
- Logged out
- Reason
- 自行鍵入
About this record
Access comprehensive regulatory information for "Inte Yakusti" Titan handheld system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 6eabc2c89e7633cca01b062a8c6728f0 and manufactured by INTERACOUSTICS A/S. The authorized representative in Taiwan is Baiou Precision Co., Ltd.
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