Taiwan FDA registration 55ca6b6b8fd5784824974716c8a75589
HOYA Vivinex multiSert Preloaded Intraocular Lens
TW: 豪雅植入器預載式單片非球面人工水晶體
Taiwan·Risk Class 3·MD·HOYA MEDICAL SINGAPORE PTE LTD·Registered Jan 13, 2020 – Jan 13, 2025ExpiredRegistration details
- Analysis ID
- 55ca6b6b8fd5784824974716c8a75589
- License Form
- Ministry of Health Medical Device Import No. 033210
- Customs Code
- DHA05603321000
Company information
- Manufacturer
- HOYA MEDICAL SINGAPORE PTE LTD
- Manufacturer Country
- Singapore
- Authorized Representative
- VIRGINIA CONTRACT RESEARCH ORGANIZATION CO., LTD.
Product details
- Product Type (Level 1)
- M Ophthalmic devices
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Jan 13, 2020
- Expiry Date
- Jan 13, 2025
- Cancellation Date
- Jun 15, 2023
About this record
Access comprehensive regulatory information for HOYA Vivinex multiSert Preloaded Intraocular Lens in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number 55ca6b6b8fd5784824974716c8a75589 and manufactured by HOYA MEDICAL SINGAPORE PTE LTD. The authorized representative in Taiwan is VIRGINIA CONTRACT RESEARCH ORGANIZATION CO., LTD..
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