Taiwan FDA registration ca6846d853b0b969c0e99807255e3221
"Hanktif" Manual Eye Surgery Instruments (Sterile/Unsterile)
TW: "瀚克提夫" 手動式眼科手術器械 (滅菌/未滅菌)
Taiwan·Risk Class 1·AKTIVE S.R.L.·Registered Nov 07, 2019 – Nov 07, 2024ExpiredRegistration details
- Analysis ID
- ca6846d853b0b969c0e99807255e3221
- Customs Code
- DHA09402101006
Company information
- Manufacturer
- AKTIVE S.R.L.
- Manufacturer Country
- Italy
- Authorized Representative
- Tiwei Wellcome Biotechnology 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
- Input;; QMS/QSD
Dates and status
- Registration Date
- Nov 07, 2019
- Expiry Date
- Nov 07, 2024
About this record
Access comprehensive regulatory information for "Hanktif" Manual Eye Surgery Instruments (Sterile/Unsterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number ca6846d853b0b969c0e99807255e3221 and manufactured by AKTIVE S.R.L.. The authorized representative in Taiwan is Tiwei Wellcome Biotechnology Co., Ltd.
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