Taiwan FDA registration df61441eb26c598e0001d99ee4bf75f0
“Rayner” Preloaded Hydrophilic Acrylic IOL Injection System
TW: “銳能” 預裝式延伸焦段非球面親水性人工水晶體推注系統
Taiwan·Risk Class 3·MD·Rayner Intraocular Lenses Limited·Registered Dec 28, 2021 – Dec 28, 2026ActiveRegistration details
- Analysis ID
- df61441eb26c598e0001d99ee4bf75f0
- License Form
- Ministry of Health Medical Device Import No. 035124
- Customs Code
- DHA05603512401
Company information
- Manufacturer
- Rayner Intraocular Lenses Limited
- Manufacturer Country
- United Kingdom
- Authorized Representative
- UNITED MEDICAL INC.
Product details
- Intended Use
- Details are as detailed as approved Chinese instructions
- Product Type (Level 1)
- M Ophthalmology
- Product Type (Level 2)
- M3600 intraocular lens
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Dec 28, 2021
- Expiry Date
- Dec 28, 2026
About this record
Access comprehensive regulatory information for “Rayner” Preloaded Hydrophilic Acrylic IOL Injection System in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number df61441eb26c598e0001d99ee4bf75f0 and manufactured by Rayner Intraocular Lenses Limited. The authorized representative in Taiwan is UNITED MEDICAL INC..
This page provides complete technical specifications, regulatory compliance details. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.
Free DatabasePowered by Pure Global AI89,000+ Devices