Taiwan FDA registration 8ca33dcd56ea6c31cf7192b2a7eb63a6
"Peisi" hearing diagnosis system
TW: “沛思”聽力診斷系統
Taiwan·Risk Class 2·PATH MEDICAL GMBH·Registered Oct 15, 2018 – Oct 15, 2028ActiveRegistration details
- Analysis ID
- 8ca33dcd56ea6c31cf7192b2a7eb63a6
- Customs Code
- DHA05603167801
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
- Oct 15, 2018
- Expiry Date
- Oct 15, 2028
About this record
Access comprehensive regulatory information for "Peisi" hearing diagnosis system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 8ca33dcd56ea6c31cf7192b2a7eb63a6 and manufactured by PATH MEDICAL GMBH. The authorized representative in Taiwan is FORMOSA MEDICAL INSTRUMENTS CO., LTD..
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