Cimosir D Gemini High Sensitivity Tube Solution
Taiwan·Risk Class 2·INSTRUMENTATION LABORATORY CO.;; BIOKIT S.A.·Registered Oct 18, 2012 – Oct 18, 2027Active- Analysis ID
- 365d171d4aed677981e9ae3c32ecdfe3
- Customs Code
- DHA00602409605
- Manufacturer
- INSTRUMENTATION LABORATORY CO.;; BIOKIT S.A.
- Manufacturer Country
- Spain;;United States
- Authorized Representative
- Werfen Taiwan Limited
- Intended Use
- Suitable for D Gemini Reagent quality control substance on ACL TOP series system.
- Product Type (Level 1)
- B Hematology, pathology, and genetics
- Product Type (Level 2)
- B.7320 Fibrinogen/Fibrinolysis Product Analysis
- Import Information
- import
- Registration Date
- Oct 18, 2012
- Expiry Date
- Oct 18, 2027
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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 365d171d4aed677981e9ae3c32ecdfe3 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.