"Torch" Cardili Mycobacterium tuberculosis rapid identification reagent (unsterilized)
Taiwan·Risk Class 1·TAUNS LABORATORIES, INC.·Registered Aug 15, 2023 – Aug 15, 2028Active- Analysis ID
- 1a0dc381fb583bd698dce982989fbf27
- Customs Code
- DHA09402320900
- Manufacturer
- TAUNS LABORATORIES, INC.
- Manufacturer Country
- Japan
- Authorized Representative
- GHOPE INTERNATIONAL BIOTECHNOLOGY CO., LTD.
- Intended Use
- Limited to the classification and grading management method of medical equipment, Mycobacterium tuberculosis immunofluorescent reagent (C.3370) first level identification range.
- Product Type (Level 1)
- C Immunology and microbiology
- Product Type (Level 2)
- C.3370 結核桿菌免疫螢光試劑
- Import Information
- Input;; QMS/QSD
- Registration Date
- Aug 15, 2023
- Expiry Date
- Aug 15, 2028
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Access comprehensive regulatory information for "Torch" Cardili Mycobacterium tuberculosis rapid identification reagent (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 1a0dc381fb583bd698dce982989fbf27 and manufactured by TAUNS LABORATORIES, INC.. The authorized representative in Taiwan is GHOPE INTERNATIONAL BIOTECHNOLOGY CO., LTD..
This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including TAUNS LABORATORIES, INC., 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.