Taiwan FDA registration 13737508e66778343eec8db5d6f79eb4
"Seiko Takagi" contrast glare tester (unsterilized)
TW: “高木精工”對比眩光測試儀 (未滅菌)
Taiwan·Risk Class 1·TAKAGI SEIKO CO., LTD.·Registered Oct 01, 2021 – Oct 31, 2025ExpiredRegistration details
- Analysis ID
- 13737508e66778343eec8db5d6f79eb4
- Customs Code
- DHA08401455407
Company information
- Manufacturer
- TAKAGI SEIKO CO., LTD.
- Manufacturer Country
- Japan
- Authorized Representative
- IKI MEDICAL CO., LTD.
Product details
- Intended Use
- Limited to the first level of recognition scope of the "Stereo Measuring Device (M.1460)" Administrative Measures for the Classification and Grading of Medical Devices.
- Product Type (Level 1)
- M Ophthalmology
- Product Type (Level 2)
- M.1460 Cubic Sense Measurer
- Import Information
- import
Dates and status
- Registration Date
- Oct 01, 2021
- Expiry Date
- Oct 31, 2025
About this record
Access comprehensive regulatory information for "Seiko Takagi" contrast glare tester (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 13737508e66778343eec8db5d6f79eb4 and manufactured by TAKAGI SEIKO CO., LTD.. The authorized representative in Taiwan is IKI MEDICAL CO., LTD..
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