Taiwan FDA registration a483498f1b921f33de97cc4508da54a4
"AIYI" manual eye surgery instruments (unsterilized)
TW: “艾依”手動式眼科手術器械 (未滅菌)
Taiwan·Risk Class 1·AMERICAN OPTISURGICAL INC.·Registered Aug 24, 2009 – Aug 24, 2014CancelledRegistration details
- Analysis ID
- a483498f1b921f33de97cc4508da54a4
- Customs Code
- DHA04400798609
Company information
- Manufacturer
- AMERICAN OPTISURGICAL INC.
- Manufacturer Country
- United States
- Authorized Representative
- BIOMEGA INSTRUMENT CO., 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
- import
Dates and status
- Registration Date
- Aug 24, 2009
- Expiry Date
- Aug 24, 2014
- Cancellation Date
- Aug 13, 2018
Cancellation information
- Status
- Logged out
- Reason
- 未展延而逾期者
About this record
Access comprehensive regulatory information for "AIYI" 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 a483498f1b921f33de97cc4508da54a4 and manufactured by AMERICAN OPTISURGICAL INC.. The authorized representative in Taiwan is BIOMEGA INSTRUMENT CO., LTD..
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