Taiwan FDA registration c1675d236088ba4b6e0c8c7be86f9e57
"AKTIVE" Manual Ophthalmic Surgical Instrument (Non-Sterile)
TW: "瀚克提夫" 手動式眼科手術器械 (未滅菌)
Taiwan·Risk Class 1·MD·AKTIVE S.R.L.·Registered Jan 10, 2019 – Jan 10, 2024ExpiredRegistration details
- Analysis ID
- c1675d236088ba4b6e0c8c7be86f9e57
- License Form
- Ministry of Health Medical Device Import No. 020012
- Customs Code
- DHA09402001205
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 Measures for the Administration of Medical Devices "Manual Eye Surgery Instruments (M.4350)".
- Product Type (Level 1)
- M Ophthalmic devices
- Product Type (Level 2)
- M4350 Manual Ophthalmic Surgery Instrument
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Jan 10, 2019
- Expiry Date
- Jan 10, 2024
About this record
Access comprehensive regulatory information for "AKTIVE" Manual Ophthalmic Surgical Instrument (Non-Sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number c1675d236088ba4b6e0c8c7be86f9e57 and manufactured by AKTIVE S.R.L.. The authorized representative in Taiwan is Tiwei Wellcome Biotechnology Co., Ltd.
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