"Io" Manual Eye Surgery Instruments (Unsterilized)
Taiwan·Risk Class 1·AMERICAN OPTISURGICAL INC.·Registered Sep 16, 2011 – Sep 16, 2026Active- Analysis ID
- ec2add808e227fb74bd325ea196bc6e4
- Customs Code
- DHA04401084402
- Manufacturer
- AMERICAN OPTISURGICAL INC.
- Manufacturer Country
- United States
- Authorized Representative
- JUN FENG OPTICAL CO., LTD.
- 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
- Registration Date
- Sep 16, 2011
- Expiry Date
- Sep 16, 2026
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Access comprehensive regulatory information for "Io" 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 ec2add808e227fb74bd325ea196bc6e4 and manufactured by AMERICAN OPTISURGICAL INC.. The authorized representative in Taiwan is JUN FENG OPTICAL CO., LTD..
This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including AMERICAN OPTISURGICAL INC., and 2 recent registrations in the same category. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.