Taiwan FDA registration 5ad0e50f38b078d9f4c5ee16efe63a14
"PATH" Senti Audiometer (Non-Sterile)
TW: "沛思" 聽力檢查儀 (未滅菌)
Taiwan·Risk Class 1·MD·PATH MEDICAL GMBH·Registered Aug 30, 2016 – Aug 30, 2026ActiveRegistration details
- Analysis ID
- 5ad0e50f38b078d9f4c5ee16efe63a14
- License Form
- Ministry of Health Medical Device Import No. 016941
- Customs Code
- DHA09401694107
Company information
- Manufacturer
- PATH MEDICAL GMBH
- Manufacturer Country
- Germany
- Authorized Representative
- FORMOSA MEDICAL INSTRUMENTS CO., LTD.
Product details
- Intended Use
- Limited to the first-level recognition range of the Measures for the Administration of Medical Devices "Audiogrammeter (G.1050)".
- Product Type (Level 1)
- G ENT device
- Product Type (Level 2)
- G1050 Audiogram
- Import Information
- Imported from abroad; GMP
Dates and status
- Registration Date
- Aug 30, 2016
- Expiry Date
- Aug 30, 2026
About this record
Access comprehensive regulatory information for "PATH" Senti Audiometer (Non-Sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 5ad0e50f38b078d9f4c5ee16efe63a14 and manufactured by PATH MEDICAL GMBH. The authorized representative in Taiwan is FORMOSA MEDICAL INSTRUMENTS CO., LTD..
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