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)
Taiwan flagTaiwan·Risk Class 1·MD·FIRSTEP BIORESEARCH INC.·Registered Nov 24, 2017 – Nov 24, 2022Expired
Registration details
Analysis ID
f80409d7c8d66779741d98d80bb50352
License Form
Ministry of Health Medical Device Manufacturing No. 007030
Company information
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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