Pure Global

“CIMA” Asteri 56 Hydrophobic Acrylic Intraocular Lens - Taiwan Registration ac1d9bd2f4381421a048cea8abe0a15a

Access comprehensive regulatory information for “CIMA” Asteri 56 Hydrophobic Acrylic 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 ac1d9bd2f4381421a048cea8abe0a15a and manufactured by CIMA Technology Inc.. The authorized representative in Taiwan is COSMOS BIO, 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 Database
Powered by Pure Global AI
89,000+ Devices
ac1d9bd2f4381421a048cea8abe0a15a
Registration Details
Taiwan FDA Registration: ac1d9bd2f4381421a048cea8abe0a15a
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing

Device Details

“CIMA” Asteri 56 Hydrophobic Acrylic Intraocular Lens
TW: “西瑪”非球面疏水性人工水晶體
Risk Class 3
MD

Registration Details

ac1d9bd2f4381421a048cea8abe0a15a

Ministry of Health Medical Device Import No. 034217

DHA05603421703

Company Information

United States

Product Details

For details, it is Chinese approved copy of the imitation order

M Ophthalmic devices

M3600 intraocular lens

Imported from abroad

Dates and Status

Dec 11, 2020

Dec 11, 2025