Taiwan FDA registration 97ba48e748073233680fc9ff19534668
"Firstep" Saliva Collection Kit (Non-Sterile)
TW: "聯華" 唾液採集盒 (未滅菌)
Taiwan·Risk Class 1·MD·FIRSTEP BIORESEARCH INC.·Registered Jul 13, 2018 – Jul 13, 2023ExpiredRegistration details
- Analysis ID
- 97ba48e748073233680fc9ff19534668
- License Form
- Ministry of Health Medical Device Manufacturing No. 007345
Company information
- Manufacturer
- FIRSTEP BIORESEARCH INC.
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- FIRSTEP BIORESEARCH INC.
Product details
- Intended Use
- Limited to the first level identification scope of the Measures for the Administration of Medical Devices "Microbial Sample Collection and Delivery Equipment (C.2900)".
- Product Type (Level 1)
- C Immunology and microbiology devices
- Product Type (Level 2)
- C2900 Microbial sample collection and delivery device
- Import Information
- Produced in Taiwan, China
Dates and status
- Registration Date
- Jul 13, 2018
- Expiry Date
- Jul 13, 2023
About this record
Access comprehensive regulatory information for "Firstep" Saliva Collection Kit (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 97ba48e748073233680fc9ff19534668 and manufactured by FIRSTEP BIORESEARCH INC.. The authorized representative in Taiwan is FIRSTEP BIORESEARCH INC..
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