Taiwan FDA registration f845f83dc545a2d095d53129567bb7cc
"Taiwan Tower" Ophthalmic Scalpel (Sterilized)
TW: “台灣參天” 眼科手術刀 (滅菌)
Taiwan·Risk Class 1·MANI,INC.·Registered Aug 18, 2021 – Aug 18, 2026ActiveRegistration details
- Analysis ID
- f845f83dc545a2d095d53129567bb7cc
- Customs Code
- DHA09402261608
Company information
- Manufacturer
- MANI,INC.
- Manufacturer Country
- Japan
- Authorized Representative
- TAIWAN SANTEN PHARMACEUTICAL 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
- QMS/QSD;; 輸入
Dates and status
- Registration Date
- Aug 18, 2021
- Expiry Date
- Aug 18, 2026
About this record
Access comprehensive regulatory information for "Taiwan Tower" Ophthalmic Scalpel (Sterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number f845f83dc545a2d095d53129567bb7cc and manufactured by MANI,INC.. The authorized representative in Taiwan is TAIWAN SANTEN PHARMACEUTICAL CO., LTD..
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