"ACRO" Flu A&B Rapid Test (Non-Sterile)
Taiwan·Risk Class 1·MD·ACRO BIOTECH. INC.·Registered Aug 30, 2016 – Aug 30, 2021Cancelled- Analysis ID
- 9e34cd8c8d9c571ce0999544c85e5578
- License Form
- Ministry of Health Medical Device Import No. 016940
- Customs Code
- DHA09401694005
- Manufacturer
- ACRO BIOTECH. INC.
- Manufacturer Country
- United States
- Authorized Representative
- Grand Marquis IVD CO., LTD.
- 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
- Aug 30, 2016
- Expiry Date
- Aug 30, 2021
- Cancellation Date
- Aug 09, 2023
- Status
- Logged out
- Reason
- 許可證已逾有效期
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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 9e34cd8c8d9c571ce0999544c85e5578 and manufactured by ACRO BIOTECH. INC.. The authorized representative in Taiwan is Grand Marquis IVD 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.