Taiwan FDA registration f80409d7c8d66779741d98d80bb50352
"Mediflora" DoA Mobile Lab_Easy Reader (Non-Sterile)
TW: 安速百爾快速試劑匣判讀機(未滅菌)
Registration details
- Analysis ID
- f80409d7c8d66779741d98d80bb50352
- License Form
- Ministry of Health Medical Device Manufacturing No. 007030
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 of identification range of "density meter/scanner for clinical use (integration, reflection, thin layer or radioactive color layer analysis)" (A.2400) under the Measures for the Administration of Medical Devices.
- Product Type (Level 1)
- A Clinical chemistry and clinical toxicology
- Product Type (Level 2)
- A2400 Density Meter/Scanner for Clinical Use (Integrated, Reflective, Thin-Layer or Radiochromatography)
- Import Information
- Produced in Taiwan, China
Dates and status
- Registration Date
- Nov 24, 2017
- Expiry Date
- Nov 24, 2022
About this record
Access comprehensive regulatory information for "Mediflora" DoA Mobile Lab_Easy Reader (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 f80409d7c8d66779741d98d80bb50352 and manufactured by FIRSTEP BIORESEARCH INC.. The authorized representative in Taiwan is FIRSTEP BIORESEARCH INC..
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