Taiwan FDA registration da18b373a688adc1beab8e012d0bdab7

“CIMA” BiVisc Sodium Hyaluronate/Sodium Chondroitin Sulfate Ophthalmic Viscosurgical Device

TW: “西瑪”雙維視人工眼內黏彈性溶液
Taiwan flagTaiwan·Risk Class 3·MD·CIMA Technology Inc.·Registered Aug 25, 2020 – Aug 25, 2025Expired
Registration details
Analysis ID
da18b373a688adc1beab8e012d0bdab7
License Form
Ministry of Health Medical Device Import No. 033897
Customs Code
DHA05603389707
Company information
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)
M4275 Liquid for intraocular filling
Import Information
Imported from abroad
Dates and status
Registration Date
Aug 25, 2020
Expiry Date
Aug 25, 2025
About this record

Access comprehensive regulatory information for “CIMA” BiVisc Sodium Hyaluronate/Sodium Chondroitin Sulfate Ophthalmic Viscosurgical Device in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number da18b373a688adc1beab8e012d0bdab7 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