Taiwan FDA registration cf9df0c2390d413a294d57bfacdd89ba
"ACRO" TB Rapid Test (Non-Sterile)
TW: "艾快露" 結核桿菌快速檢驗試劑 (未滅菌)
Taiwan·Risk Class 1·MD·ACRO BIOTECH. INC.·Registered Sep 10, 2016 – Sep 10, 2021CancelledRegistration details
- Analysis ID
- cf9df0c2390d413a294d57bfacdd89ba
- License Form
- Ministry of Health Medical Device Import No. 016994
- Customs Code
- DHA09401699402
Company information
- Manufacturer
- ACRO BIOTECH. INC.
- Manufacturer Country
- United States
- Authorized Representative
- Grand Marquis IVD CO., LTD.
Product details
- Product Type (Level 1)
- C Immunology and microbiology devices
- Product Type (Level 2)
- C3370 Mycobacterium tuberculosis immunofluorescent reagent
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Sep 10, 2016
- Expiry Date
- Sep 10, 2021
- Cancellation Date
- Aug 09, 2023
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "ACRO" TB 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 cf9df0c2390d413a294d57bfacdd89ba and manufactured by ACRO BIOTECH. INC.. The authorized representative in Taiwan is Grand Marquis IVD CO., LTD..
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