Taiwan FDA registration 30cf896dd85cc82d3f71f3e1e92a7660
"Dell" Manual Eye Surgery Instruments (Unsterilized)
TW: "戴爾" 手動式眼科手術器械(未滅菌)
Taiwan·Risk Class 1·DIAMATRIX LTD·Registered Feb 02, 2023 – Feb 02, 2028ActiveRegistration details
- Analysis ID
- 30cf896dd85cc82d3f71f3e1e92a7660
- Customs Code
- DHA09402303101
Company information
- Manufacturer
- DIAMATRIX LTD
- Manufacturer Country
- United States
- Authorized Representative
- CONEYE CO., LTD
Product details
- Intended Use
- Limited to the first level identification scope of the "Manual Ophthalmic Surgical Instruments (M.4350)" of the Measures for the Classification and Grading of Medical Equipment.
- Product Type (Level 1)
- M Ophthalmology
- Product Type (Level 2)
- M.4350 手動式眼科手術器械
- Import Information
- QMS/QSD;; 輸入
Dates and status
- Registration Date
- Feb 02, 2023
- Expiry Date
- Feb 02, 2028
About this record
Access comprehensive regulatory information for "Dell" Manual Eye Surgery Instruments (Unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 30cf896dd85cc82d3f71f3e1e92a7660 and manufactured by DIAMATRIX LTD. The authorized representative in Taiwan is CONEYE CO., LTD.
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