Taiwan FDA registration 367d12bc083643acbeca2a03cbb41c09
Cimosir Apixaban correction liquid and quality control fluid
TW: 希摩西爾 Apixaban校正液及品管液
Taiwan·Risk Class 2·INSTRUMENTATION LABORATORY CO.·Registered Jul 18, 2018 – Jul 18, 2028ActiveRegistration details
- Analysis ID
- 367d12bc083643acbeca2a03cbb41c09
- Customs Code
- DHA05603133507
Company information
- Manufacturer
- INSTRUMENTATION LABORATORY CO.
- Manufacturer Country
- United States
- Authorized Representative
- Werfen Taiwan Limited
Product details
- Intended Use
- This product calibration solution can be used for correction by ACL TOP Family when performing Apixaban's Liquid Anti-Xa test. This product quality control liquid can be used for quality control when ACL TOP Family conducts Apixaban's Liquid Anti-Xa test.
- Product Type (Level 1)
- A Clinical chemistry and clinical toxicology
- Product Type (Level 2)
- A.1660 Quality control materials (analytical and non-analytical); A.1150 calibration
- Import Information
- import
Dates and status
- Registration Date
- Jul 18, 2018
- Expiry Date
- Jul 18, 2028
About this record
Access comprehensive regulatory information for Cimosir Apixaban correction liquid and quality control fluid in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 367d12bc083643acbeca2a03cbb41c09 and manufactured by INSTRUMENTATION LABORATORY CO.. The authorized representative in Taiwan is Werfen Taiwan Limited.
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