Taiwan FDA registration 45489a9597434690950ec77c86f5f5e0

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

TW: “視瑪”人工玻璃體

Taiwan·Risk Class 3·MD·CIMA Technology Inc.·Registered Nov 09, 2016 – Nov 09, 2021Cancelled

Registration details

Analysis ID: 45489a9597434690950ec77c86f5f5e0
License Form: Ministry of Health Medical Device Import No. 028896
Customs Code: DHA05602889601

Company information

Manufacturer: CIMA Technology Inc.
Manufacturer Country: United States
Authorized Representative: UNITED MEDICAL INC.

Product details

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: Nov 09, 2016
Expiry Date: Nov 09, 2021
Cancellation Date: Sep 09, 2021

Cancellation information

Status: Logged out
Reason: 自請註銷

About this record

Access comprehensive regulatory information for “CIMA” 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 45489a9597434690950ec77c86f5f5e0 and manufactured by CIMA Technology Inc.. 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.