Taiwan FDA registration 28f770004016f75fbe240037d4fecf31
“HUMANOPTICS” Acrylic Intraocular Lens Aspira-aXA
TW: “優眼光學”優視非球面人工水晶體
Taiwan·Risk Class 3·MD·HumanOptics Holding AG·Registered Dec 23, 2020 – Dec 23, 2025ExpiredRegistration details
- Analysis ID
- 28f770004016f75fbe240037d4fecf31
- License Form
- Ministry of Health Medical Device Import No. 034229
- Customs Code
- DHA05603422900
Company information
- Manufacturer
- HumanOptics Holding AG
- Manufacturer Country
- Germany
- Authorized Representative
- MEDBEST ENTERPRISE CO., LTD.
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- M Ophthalmic devices
- Product Type (Level 2)
- M3600 intraocular lens
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Dec 23, 2020
- Expiry Date
- Dec 23, 2025
About this record
Access comprehensive regulatory information for “HUMANOPTICS” Acrylic Intraocular Lens Aspira-aXA in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number 28f770004016f75fbe240037d4fecf31 and manufactured by HumanOptics Holding AG. The authorized representative in Taiwan is MEDBEST ENTERPRISE CO., LTD..
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