Taiwan FDA registration 42e7553e9dbda7c97c46cb6fcba1f32d
"Taiwan tower" anterior chamber catheter (sterilized)
TW: “台灣參天” 前房導管 (滅菌)
Taiwan·Risk Class 1·PSI/EYE-KO, Inc. dba Anodyne Surgical·Registered Jun 21, 2023 – Jun 21, 2028ActiveRegistration details
- Analysis ID
- 42e7553e9dbda7c97c46cb6fcba1f32d
- Customs Code
- DHA09402315901
Company information
- Manufacturer
- PSI/EYE-KO, Inc. dba Anodyne Surgical
- Manufacturer Country
- United States
- 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
- Jun 21, 2023
- Expiry Date
- Jun 21, 2028
About this record
Access comprehensive regulatory information for "Taiwan tower" anterior chamber catheter (sterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 42e7553e9dbda7c97c46cb6fcba1f32d and manufactured by PSI/EYE-KO, Inc. dba Anodyne Surgical. The authorized representative in Taiwan is TAIWAN SANTEN PHARMACEUTICAL CO., LTD..
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