Taiwan FDA registration d0ee5f91d92504f826eff36c43a1298e
"DeXscope" Otoscope(Non-sterile)
TW: "帝視寰宇" 耳鏡 (未滅菌)
Taiwan·Risk Class 1·MD·DEX MEDICAL DEVICE CO., LTD.·Registered Sep 23, 2019 – Sep 23, 2024ExpiredRegistration details
- Analysis ID
- d0ee5f91d92504f826eff36c43a1298e
- License Form
- Ministry of Health Medical Device Manufacturing No. 007968
Company information
- Manufacturer
- DEX MEDICAL DEVICE CO., LTD.
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- DEX MEDICAL DEVICE CO., LTD.
Product details
- Intended Use
- Limited to the first level identification range of the Measures for the Administration of Medical Devices "Otoscope (G.4770)".
- Product Type (Level 1)
- G ENT device
- Product Type (Level 2)
- G4770 Otoscope
- Import Information
- Produced in Taiwan, China
Dates and status
- Registration Date
- Sep 23, 2019
- Expiry Date
- Sep 23, 2024
About this record
Access comprehensive regulatory information for "DeXscope" Otoscope(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 d0ee5f91d92504f826eff36c43a1298e and manufactured by DEX MEDICAL DEVICE CO., LTD.. The authorized representative in Taiwan is DEX MEDICAL DEVICE CO., LTD..
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