"Torch" Cardili Mycobacterium tuberculosis rapid identification reagent (unsterilized)
Taiwan·Risk Class 1·TAUNS LABORATORIES, INC.·Registered Jul 10, 2013 – Jul 10, 2023Expired- Analysis ID
- cfa4c8d282a0d2b51871d2eeb8a1424c
- Customs Code
- DHA04401319302
- Manufacturer
- TAUNS LABORATORIES, INC.
- Manufacturer Country
- Japan
- Authorized Representative
- GHOPE INTERNATIONAL BIOTECHNOLOGY CO., LTD.
- Intended Use
- Limited to the first level identification range of Mycobacterium tuberculosis immunofluorescent reagent (C.3370) of the management method for medical devices.
- 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
- import
- Registration Date
- Jul 10, 2013
- Expiry Date
- Jul 10, 2023
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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 cfa4c8d282a0d2b51871d2eeb8a1424c 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.