Taiwan FDA registration b80b53fe06af95d3272759a90578cc1d
"Archimi" Haibo intraocular liquid substitutes and accessories
TW: “阿基米”海博眼內液體替代物及配件
Taiwan·Risk Class 3·AL. CHI.MI.A. S.R.L.·Registered Dec 23, 2011 – Dec 23, 2026ActiveRegistration details
- Analysis ID
- b80b53fe06af95d3272759a90578cc1d
- Customs Code
- DHA00602314500
Company information
- Manufacturer
- AL. CHI.MI.A. S.R.L.
- Manufacturer Country
- Italy
- Authorized Representative
- SUNNY MEDICAL INC.
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- M Ophthalmology
- Product Type (Level 2)
- M.4275 眼內充填用液體
- Import Information
- import
Dates and status
- Registration Date
- Dec 23, 2011
- Expiry Date
- Dec 23, 2026
About this record
Access comprehensive regulatory information for "Archimi" Haibo intraocular liquid substitutes and accessories in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number b80b53fe06af95d3272759a90578cc1d and manufactured by AL. CHI.MI.A. S.R.L.. The authorized representative in Taiwan is SUNNY MEDICAL INC..
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