Taiwan FDA registration 6387f9682694e04ffeaab90f5c929ad9
Romes Manual Eye Surgery Instruments (Unsterilized)
TW: “羅美思”手動式眼科手術器械 (未滅菌)
Registration details
- Analysis ID
- 6387f9682694e04ffeaab90f5c929ad9
- Customs Code
- DHA04400807308
Company information
- Manufacturer
- RUMEX INTERNATIONAL COMPANY
- Manufacturer Country
- United States
- Authorized Representative
- BIOMEGA INSTRUMENT 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
- import
Dates and status
- Registration Date
- Sep 11, 2009
- Expiry Date
- Sep 11, 2024
About this record
Access comprehensive regulatory information for Romes 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 6387f9682694e04ffeaab90f5c929ad9 and manufactured by RUMEX INTERNATIONAL COMPANY. The authorized representative in Taiwan is BIOMEGA INSTRUMENT CO., LTD..
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