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“Rayner”Aspheric Acrylic IOL with RaySert PLUS - Taiwan Registration df7fe93b11fb1b30bdae913c8bc7f7c9

Access comprehensive regulatory information for “Rayner”Aspheric Acrylic IOL with RaySert PLUS in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number df7fe93b11fb1b30bdae913c8bc7f7c9 and manufactured by RAYNER INTRAOCULAR LENSES LTD.. 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.

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df7fe93b11fb1b30bdae913c8bc7f7c9
Registration Details
Taiwan FDA Registration: df7fe93b11fb1b30bdae913c8bc7f7c9
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Device Details

“Rayner”Aspheric Acrylic IOL with RaySert PLUS
TW: “銳能”非球面推注式人工水晶體系統
Risk Class 3
MD
Cancelled

Registration Details

df7fe93b11fb1b30bdae913c8bc7f7c9

Ministry of Health Medical Device Import No. 026560

DHA05602656007

Company Information

United Kingdom

Product Details

M Ophthalmic devices

M3600 intraocular lens

Imported from abroad

Dates and Status

Sep 12, 2014

Sep 12, 2019

Jun 22, 2022

Cancellation Information

Logged out

許可證已逾有效期