Taiwan FDA registration 344f05a238dca65caf6c86458b4368c9
"Kaile" Vision Tester and Accessories (Unsterilized)
TW: "凱樂" 視力檢查儀及附件 (未滅菌)
Taiwan·Risk Class 1·KEELER LTD.·Registered May 25, 2012 – May 25, 2027ActiveRegistration details
- Analysis ID
- 344f05a238dca65caf6c86458b4368c9
- Customs Code
- DHA04401175008
Company information
- Manufacturer
- KEELER LTD.
- Manufacturer Country
- United Kingdom
- Authorized Representative
- TAIWAN OPTICAL CO., LTD.
Product details
- Intended Use
- Limited to the first level identification scope of the "Ophthalmic Projector (M.1680)" of the Measures for the Classification and Grading of Medical Equipment.
- Product Type (Level 1)
- M Ophthalmology
- Product Type (Level 2)
- M.1680 眼科用投影機
- Import Information
- import
Dates and status
- Registration Date
- May 25, 2012
- Expiry Date
- May 25, 2027
About this record
Access comprehensive regulatory information for "Kaile" Vision Tester and Accessories (Unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 344f05a238dca65caf6c86458b4368c9 and manufactured by KEELER LTD.. The authorized representative in Taiwan is TAIWAN OPTICAL CO., LTD..
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