Taiwan FDA registration f62e5a751635e62282ab398d0bc40545
"Ness" battery-powered retinoscope (unsterilized)
TW: "奈斯" 電池供電式視網膜鏡 (未滅菌)
Taiwan·Risk Class 1·NEITZ INSTRUMENTS CO., LTD.·Registered Jul 17, 2019 – Jul 17, 2024ExpiredRegistration details
- Analysis ID
- f62e5a751635e62282ab398d0bc40545
- Customs Code
- DHA09402065600
Company information
- Manufacturer
- NEITZ INSTRUMENTS CO., LTD.
- Manufacturer Country
- Japan
- Authorized Representative
- Kangcheng Biomedical Technology Co., Ltd
Product details
- Intended Use
- Limited to the classification and grading management of medical equipment "Retinal Scope (M.1780) First Grade Identification Range.
- Product Type (Level 1)
- M Ophthalmology
- Product Type (Level 2)
- M.1780 Retinal Lens
- Import Information
- QMS/QSD;; 輸入
Dates and status
- Registration Date
- Jul 17, 2019
- Expiry Date
- Jul 17, 2024
About this record
Access comprehensive regulatory information for "Ness" battery-powered retinoscope (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number f62e5a751635e62282ab398d0bc40545 and manufactured by NEITZ INSTRUMENTS CO., LTD.. The authorized representative in Taiwan is Kangcheng Biomedical Technology Co., Ltd.
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