Cimosir D Gemini High Sensitivity Tube Solution
Taiwan·Risk Class 2·INSTRUMENTATION LABORATORY CO.;; BIOKIT S.A.·Registered Apr 13, 2022 – Apr 13, 2027Active- Analysis ID
- 885b459a73b4d81c8c78c50ce0d962fd
- Customs Code
- DHA05603523905
- Manufacturer
- INSTRUMENTATION LABORATORY CO.;; BIOKIT S.A.
- Manufacturer Country
- Spain;;United States
- Authorized Representative
- Werfen Taiwan Limited
- Intended Use
- For quality control of HemosIL D-Dimer HS 500 analysis on the ACL TOP Family system.
- Product Type (Level 1)
- A Clinical chemistry and clinical toxicology
- Product Type (Level 2)
- A.1660 Quality control materials (analytical and non-analytical)
- Import Information
- QMS/QSD;; 委託製造;; 輸入
- Registration Date
- Apr 13, 2022
- Expiry Date
- Apr 13, 2027
Top companies providing products similar to "Cimosir D Gemini High Sensitivity Tube Solution"
Recently registered similar products
Access comprehensive regulatory information for Cimosir D Gemini High Sensitivity Tube Solution in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 885b459a73b4d81c8c78c50ce0d962fd and manufactured by INSTRUMENTATION LABORATORY CO.;; BIOKIT S.A.. The authorized representative in Taiwan is Werfen Taiwan Limited.
This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including INSTRUMENTATION LABORATORY CO.;; BIOKIT S.A., and 1 recent registrations in the same category. 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.