Taiwan FDA registration 834d83912e286b3864ee1913df6fe81c
“Rayner” OphteisBio Viscoelastic sodium hyaluronate solution
TW: “銳能”歐福視百黏彈體
Taiwan·Risk Class 3·MD·Rayner Intraocular Lenses Limited·Registered Nov 14, 2019 – Nov 14, 2024ExpiredRegistration details
- Analysis ID
- 834d83912e286b3864ee1913df6fe81c
- License Form
- Ministry of Health Medical Device Import No. 032920
- Customs Code
- DHA05603292000
Company information
- Manufacturer
- Rayner Intraocular Lenses Limited
- Manufacturer Country
- United Kingdom
- Authorized Representative
- UNITED MEDICAL INC.
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)
- M4275 Liquid for intraocular filling
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Nov 14, 2019
- Expiry Date
- Nov 14, 2024
About this record
Access comprehensive regulatory information for “Rayner” OphteisBio Viscoelastic sodium hyaluronate solution in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number 834d83912e286b3864ee1913df6fe81c and manufactured by Rayner Intraocular Lenses Limited. The authorized representative in Taiwan is UNITED MEDICAL INC..
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