Taiwan FDA registration 0f26dd5c255ac561b0570cc76dbd63fd
"Neis" battery-powered retinoscope (unsterilized)
TW: “耐司” 電池供電式視網膜鏡 (未滅菌)
Taiwan·Risk Class 1·NEITZ INSTRUMENTS CO., LTD.·Registered Feb 03, 2021 – Feb 03, 2026ExpiredRegistration details
- Analysis ID
- 0f26dd5c255ac561b0570cc76dbd63fd
- Customs Code
- DHA09402229402
Company information
- Manufacturer
- NEITZ INSTRUMENTS CO., LTD.
- Manufacturer Country
- Japan
- Authorized Representative
- BIOMEGA INSTRUMENT 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
- Input;; QMS/QSD
Dates and status
- Registration Date
- Feb 03, 2021
- Expiry Date
- Feb 03, 2026
About this record
Access comprehensive regulatory information for "Neis" 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 0f26dd5c255ac561b0570cc76dbd63fd and manufactured by NEITZ INSTRUMENTS CO., LTD.. The authorized representative in Taiwan is BIOMEGA INSTRUMENT CO., LTD..
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