Taiwan FDA registration 36e58a68efce7c57f868001ba5edc774
“Rayner” Advance Preloaded Hydrophilic Acrylic IOL Injection System
TW: “銳能”進階推注式非球面人工水晶體系統
Taiwan·Risk Class 3·MD·RAYNER INTRAOCULAR LENSES LTD.·Registered May 26, 2014 – May 26, 2019CancelledRegistration details
- Analysis ID
- 36e58a68efce7c57f868001ba5edc774
- License Form
- Ministry of Health Medical Device Import No. 026216
- Customs Code
- DHA05602621605
Company information
- Manufacturer
- RAYNER INTRAOCULAR LENSES LTD.
- Manufacturer Country
- United Kingdom
- Authorized Representative
- UNITED MEDICAL INC.
Product details
- Product Type (Level 1)
- M Ophthalmic devices
- Product Type (Level 2)
- M3600 intraocular lens
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- May 26, 2014
- Expiry Date
- May 26, 2019
- Cancellation Date
- Jun 22, 2022
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for “Rayner” Advance 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 36e58a68efce7c57f868001ba5edc774 and manufactured by RAYNER INTRAOCULAR LENSES LTD.. The authorized representative in Taiwan is UNITED MEDICAL INC..
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