Taiwan FDA registration c40f96d7478efe2fabe9cb983b436ac2
"Agility" manual ophthalmic surgery instrument (sterile)
TW: "敏能" 手動式眼科手術器械 (滅菌)
Taiwan·Risk Class 1·MANI INC.·Registered May 02, 2012 – May 02, 2027ActiveRegistration details
- Analysis ID
- c40f96d7478efe2fabe9cb983b436ac2
- Customs Code
- DHA04401165402
Company information
- Manufacturer
- MANI INC.
- Manufacturer Country
- Japan
- Authorized Representative
- UNITED MEDICAL INC.
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;; 輸入
Dates and status
- Registration Date
- May 02, 2012
- Expiry Date
- May 02, 2027
About this record
Access comprehensive regulatory information for "Agility" manual ophthalmic surgery instrument (sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number c40f96d7478efe2fabe9cb983b436ac2 and manufactured by MANI INC.. The authorized representative in Taiwan is UNITED MEDICAL INC..
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