Taiwan FDA registration 3c50e6e987ad73c99b53b94d00ae956f
ENNOLIFE Microalbumin (mALB) Test (Non-Sterile)
TW: 伊諾來富 微白蛋白試劑 (未滅菌)
Taiwan·Risk Class 1·MD·PROTECTLIFE INTERNATIONAL BIOMEDICAL INC.·Registered Sep 14, 2018 – Sep 14, 2028ActiveRegistration details
- Analysis ID
- 3c50e6e987ad73c99b53b94d00ae956f
- License Form
- Ministry of Health Medical Device Manufacturing No. 007428
Company information
- Manufacturer
- PROTECTLIFE INTERNATIONAL BIOMEDICAL INC.
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- PROTECTLIFE INTERNATIONAL BIOMEDICAL INC.
Product details
- Intended Use
- Limited to the first level recognition range of the "albumin immunoassay system (C.5040)" of the Measures for the Administration of Medical Devices.
- Product Type (Level 1)
- C Immunology and microbiology devices
- Product Type (Level 2)
- C5040 Albumin immunoassay system
- Import Information
- Produced in Taiwan, China
Dates and status
- Registration Date
- Sep 14, 2018
- Expiry Date
- Sep 14, 2028
About this record
Access comprehensive regulatory information for ENNOLIFE Microalbumin (mALB) Test (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 3c50e6e987ad73c99b53b94d00ae956f and manufactured by PROTECTLIFE INTERNATIONAL BIOMEDICAL INC.. The authorized representative in Taiwan is PROTECTLIFE INTERNATIONAL BIOMEDICAL INC..
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