Taiwan FDA registration d702b63a81f7ae7ebf2886db3bd184b3
"Peisi" multi-function induction hearing examiner
TW: “沛思”多功能誘發聽力檢查儀
Taiwan·Risk Class 2·PATH MEDICAL GMBH·Registered Sep 05, 2018 – Sep 05, 2028ActiveRegistration details
- Analysis ID
- d702b63a81f7ae7ebf2886db3bd184b3
- Customs Code
- DHA05603159102
Company information
- Manufacturer
- PATH MEDICAL GMBH
- Manufacturer Country
- Germany
- Authorized Representative
- FORMOSA MEDICAL INSTRUMENTS 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
- Sep 05, 2018
- Expiry Date
- Sep 05, 2028
About this record
Access comprehensive regulatory information for "Peisi" multi-function induction hearing examiner in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number d702b63a81f7ae7ebf2886db3bd184b3 and manufactured by PATH MEDICAL GMBH. The authorized representative in Taiwan is FORMOSA MEDICAL INSTRUMENTS CO., LTD..
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