"ACRO" Flu A&B Rapid Test (Non-Sterile)
Taiwan·Risk Class 1·MD·ACRO BIOTECH. INC.·Registered Jan 16, 2017 – Jan 16, 2022Expired- Analysis ID
- e9275fee5ef6e5700d71b4fdde4427c2
- License Form
- Ministry of Health Medical Device Import No. 017416
- Customs Code
- DHA09401741606
- Manufacturer
- ACRO BIOTECH. INC.
- Manufacturer Country
- United States
- Authorized Representative
- APPLIED BIOTECH ENTERPRISE CO., LTD.
- Intended Use
- Limited to the first level identification range of the Measures for the Administration of Medical Devices "Influenza Virus Serum Reagent (C.3330)".
- Product Type (Level 1)
- C Immunology and microbiology devices
- Product Type (Level 2)
- C3330 Influenza virus serum reagent
- Import Information
- Imported from abroad
- Registration Date
- Jan 16, 2017
- Expiry Date
- Jan 16, 2022
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Access comprehensive regulatory information for "ACRO" Flu A&B Rapid Test (Non-Sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number e9275fee5ef6e5700d71b4fdde4427c2 and manufactured by ACRO BIOTECH. INC.. The authorized representative in Taiwan is APPLIED BIOTECH ENTERPRISE CO., LTD..
This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including ACRO BIOTECH. 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.