Taiwan FDA registration 17a6d38e1bed2d5afb09e8b720151956
"Akihito" manual ophthalmic surgical instrument (not sterilized)
TW: “明仁”手動式眼科手術器械 (未滅菌)
Taiwan·Risk Class 1·MINGREN OPHTHALMIC INSTRUMENTS CO., LTD.·Registered Nov 26, 2007 – Nov 26, 2022CancelledRegistration details
- Analysis ID
- 17a6d38e1bed2d5afb09e8b720151956
- Customs Code
- DHA04600045804
Company information
- Manufacturer
- MINGREN OPHTHALMIC INSTRUMENTS CO., LTD.
- Manufacturer Country
- China
- Authorized Representative
- OCARE LTD.
Product details
- Intended Use
- Limited to the first level identification scope of the Measures for the Administration of Medical Devices "Manual Eye Surgery Instruments (M.4350)".
- Product Type (Level 1)
- M Ophthalmology
- Product Type (Level 2)
- M.4350 手動式眼科手術器械
- Import Information
- Chinese goods;; input
Dates and status
- Registration Date
- Nov 26, 2007
- Expiry Date
- Nov 26, 2022
- Cancellation Date
- Apr 12, 2024
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Akihito" manual ophthalmic surgical instrument (not sterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 17a6d38e1bed2d5afb09e8b720151956 and manufactured by MINGREN OPHTHALMIC INSTRUMENTS CO., LTD.. The authorized representative in Taiwan is OCARE LTD..
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