Taiwan FDA registration 1a80b7860101c735e9522a3140547d0a
〝Disposcope〞Speculum and Accessories(Non-Sterile)
TW: 〝帝視寰宇〞檢查鏡及其附件 (未滅菌)
Taiwan·Risk Class 1·MD·DEX MEDICAL DEVICE CO., LTD.·Registered Oct 07, 2019 – Oct 07, 2024ExpiredRegistration details
- Analysis ID
- 1a80b7860101c735e9522a3140547d0a
- License Form
- Ministry of Health Medical Device Manufacturing No. 007985
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 "Examination Scopes and Their Accessories (I.1800)".
- Product Type (Level 1)
- I General and plastic surgical devices
- Product Type (Level 2)
- I1800 inspection mirror and accessories
- Import Information
- Produced in Taiwan, China
Dates and status
- Registration Date
- Oct 07, 2019
- Expiry Date
- Oct 07, 2024
About this record
Access comprehensive regulatory information for 〝Disposcope〞Speculum and Accessories(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 1a80b7860101c735e9522a3140547d0a and manufactured by DEX MEDICAL DEVICE CO., LTD.. The authorized representative in Taiwan is DEX MEDICAL DEVICE CO., LTD..
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