Taiwan FDA registration 5fc998b04713805797f65cdee45ea1bf
"Likuan" Legionnaires' Pneumonia Antigen Urine Test Reagent (Unsterilized)
TW: "立寬" 退伍軍人症肺炎抗原尿液檢驗試劑 (未滅菌)
Taiwan·Risk Class 1·AMERITEK·Registered Aug 08, 2014 – Aug 08, 2019CancelledRegistration details
- Analysis ID
- 5fc998b04713805797f65cdee45ea1bf
- Customs Code
- DHA09600219106
Company information
- Manufacturer
- AMERITEK
- Manufacturer Country
- China
- Authorized Representative
- LIKWANG INSTRUMENTS 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
- Product Type (Level 2)
- C.3300 嗜血桿菌屬血清試劑
- Import Information
- Input;; Chinese goods
Dates and status
- Registration Date
- Aug 08, 2014
- Expiry Date
- Aug 08, 2019
- Cancellation Date
- Jun 22, 2022
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Likuan" Legionnaires' Pneumonia Antigen Urine Test 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 5fc998b04713805797f65cdee45ea1bf and manufactured by AMERITEK. The authorized representative in Taiwan is LIKWANG INSTRUMENTS CO., LTD..
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