Taiwan FDA registration e66f539a6d3b841b80a79f5dc38db789
"Aofo" Manual Eye Surgery Instruments (Unsterilized)
TW: “澳福” 手動式眼科手術器械(未滅菌)
Taiwan·Risk Class 1·HUAIAN WOLFRAM SURGICAL INSTRUMENTS CO., LTD.·Registered Oct 25, 2010 – Oct 25, 2025ExpiredRegistration details
- Analysis ID
- e66f539a6d3b841b80a79f5dc38db789
- Customs Code
- DHA04600110400
Company information
- Manufacturer
- HUAIAN WOLFRAM SURGICAL INSTRUMENTS CO., LTD.
- Manufacturer Country
- China
- Authorized Representative
- RAY HUNG 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
- Chinese goods;; input
Dates and status
- Registration Date
- Oct 25, 2010
- Expiry Date
- Oct 25, 2025
About this record
Access comprehensive regulatory information for "Aofo" 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 e66f539a6d3b841b80a79f5dc38db789 and manufactured by HUAIAN WOLFRAM SURGICAL INSTRUMENTS CO., LTD.. The authorized representative in Taiwan is RAY HUNG INSTRUMENT CO., LTD..
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