Taiwan FDA registration f34230e8894ce52207dc0601975d44cb
"Lu Meisi" Manual Ophthalmic Surgery Instrument (Sterile)
TW: "路美思" 手動式眼科手術器械 (滅菌)
Registration details
- Analysis ID
- f34230e8894ce52207dc0601975d44cb
- Customs Code
- DHA09402053804
Company information
- Manufacturer
- RUMEX INTERNATIONAL LTD
- Manufacturer Country
- United Kingdom
- 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
- Jun 12, 2019
- Expiry Date
- Jun 12, 2029
About this record
Access comprehensive regulatory information for "Lu Meisi" Manual Ophthalmic Surgery Instrument (Sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number f34230e8894ce52207dc0601975d44cb and manufactured by RUMEX INTERNATIONAL LTD. The authorized representative in Taiwan is CONEYE CO., LTD.
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