Taiwan FDA registration ac1d9bd2f4381421a048cea8abe0a15a
“CIMA” Asteri 56 Hydrophobic Acrylic Intraocular Lens
TW: “西瑪”非球面疏水性人工水晶體
Taiwan·Risk Class 3·MD·CIMA Technology Inc.·Registered Dec 11, 2020 – Dec 11, 2025ExpiredRegistration details
- Analysis ID
- ac1d9bd2f4381421a048cea8abe0a15a
- License Form
- Ministry of Health Medical Device Import No. 034217
- Customs Code
- DHA05603421703
Company information
- Manufacturer
- CIMA Technology Inc.
- Manufacturer Country
- United States
- Authorized Representative
- COSMOS BIO, 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)
- M3600 intraocular lens
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Dec 11, 2020
- Expiry Date
- Dec 11, 2025
About this record
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 DatabasePowered by Pure Global AI89,000+ Devices