Taiwan FDA registration 6de84a63ecca4ecbf35565451fcd5911
"Taiyang" Battle Respiratory Virus Screening and Identification Kit (Unsterilized)
TW: "太暘" 巴特爾 呼吸道病毒篩選和鑑定試劑組 (未滅菌)
Taiwan·Risk Class 1·TRINITY BIOTECH PLC·Registered Dec 13, 2011 – Dec 13, 2021CancelledRegistration details
- Analysis ID
- 6de84a63ecca4ecbf35565451fcd5911
- Customs Code
- DHA04401117003
Company information
- Manufacturer
- TRINITY BIOTECH PLC
- Manufacturer Country
- Ireland
- Authorized Representative
- EVERLIGHT BIOTECH(TAIWAN) CO., LTD.
Product details
- 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
- Product Type (Level 2)
- C.3330 流感病毒血清試劑
- Import Information
- import
Dates and status
- Registration Date
- Dec 13, 2011
- Expiry Date
- Dec 13, 2021
- Cancellation Date
- Aug 15, 2023
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Taiyang" Battle Respiratory Virus Screening and Identification Kit (Unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 6de84a63ecca4ecbf35565451fcd5911 and manufactured by TRINITY BIOTECH PLC. The authorized representative in Taiwan is EVERLIGHT BIOTECH(TAIWAN) CO., LTD..
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