Taiwan FDA registration 281253f6e8e13255dca33d7347c61dc7
"Cai Ji" Manual Ophthalmic Surgery Instrument (Sterile)
TW: “蔡司” 手動式眼科手術器械 (滅菌)
Taiwan·Risk Class 1·CARL ZEISS MEDITEC AG;; COASTLINE DE MEXICO, S.A. DE C.V.·Registered Jan 06, 2021 – Jan 06, 2026ExpiredRegistration details
- Analysis ID
- 281253f6e8e13255dca33d7347c61dc7
- Customs Code
- DHA09402222302
Company information
- Manufacturer Country
- Mexico;;Germany
- Authorized Representative
- Carl Zeiss Co., Ltd. Taipei Branch
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
- 委託製造;; QMS/QSD;; 輸入
Dates and status
- Registration Date
- Jan 06, 2021
- Expiry Date
- Jan 06, 2026
About this record
Access comprehensive regulatory information for "Cai Ji" 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 281253f6e8e13255dca33d7347c61dc7 and manufactured by CARL ZEISS MEDITEC AG;; COASTLINE DE MEXICO, S.A. DE C.V.. The authorized representative in Taiwan is Carl Zeiss Co., Ltd. Taipei Branch.
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