Taiwan FDA registration ce91f66a6a22e3dde986c471ec6b2786
"Akihito" manual ophthalmic surgical instrument (unsterilized)
TW: "明仁" 手動式眼科手術器械 (未滅菌)
Registration details
- Analysis ID
- ce91f66a6a22e3dde986c471ec6b2786
- Customs Code
- DHA09600470801
Company information
- Manufacturer Country
- China
- Authorized Representative
- OCARE 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;; Input;; Chinese goods;; Contract manufacturing
Dates and status
- Registration Date
- Dec 12, 2022
- Expiry Date
- Dec 12, 2027
About this record
Access comprehensive regulatory information for "Akihito" manual ophthalmic surgical instrument (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number ce91f66a6a22e3dde986c471ec6b2786 and manufactured by Mingren Ophthalmic Instruments Co., Ltd.;; Xiehe Medical Instruments.. The authorized representative in Taiwan is OCARE LTD..
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