Taiwan FDA registration 0dc781c9dd9d4bb21d0b3049ae1d7ce3
"AMERITEK" Legionella-Ag test (Non-Sterile)
TW: "爾美力特克" 退伍軍人肺炎抗原檢驗試劑 (未滅菌)
Taiwan·Risk Class 1·MD·AMERITEK, INC.·Registered Nov 29, 2013 – Nov 29, 2023ExpiredRegistration details
- Analysis ID
- 0dc781c9dd9d4bb21d0b3049ae1d7ce3
- License Form
- Ministry of Health Medical Device Import No. 013645
- Customs Code
- DHA09401364501
Company information
- Manufacturer
- AMERITEK, INC.
- Manufacturer Country
- United States
- Authorized Representative
- APPLIED BIOTECH ENTERPRISE CO., LTD.
Product details
- Intended Use
- Limit the management method of medical equipment Haemophilus serogenus (C.3300) first level identification range.
- Product Type (Level 1)
- C Immunology and microbiology devices
- Product Type (Level 2)
- C3300 Haemophilus serology
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Nov 29, 2013
- Expiry Date
- Nov 29, 2023
About this record
Access comprehensive regulatory information for "AMERITEK" Legionella-Ag 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 0dc781c9dd9d4bb21d0b3049ae1d7ce3 and manufactured by AMERITEK, INC.. The authorized representative in Taiwan is APPLIED BIOTECH ENTERPRISE CO., LTD..
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