Taiwan FDA registration 03bc0f7d3ef0b047dd537676c5686d53

“Medica” Albumin Reagent Kit (ALB)

TW: “美麗佳” 白蛋白試劑
Taiwan flagTaiwan·Risk Class 2·MD·MEDICA CORPORATION·Registered Jan 27, 2014 – Jan 27, 2024Expired
Registration details
Analysis ID
03bc0f7d3ef0b047dd537676c5686d53
License Form
Ministry of Health Medical Device Import No. 025866
Customs Code
DHA05602586600
Company information
Manufacturer
MEDICA CORPORATION
Manufacturer Country
United States
Authorized Representative
GRAND MARQUIS CO., LTD.
Product details
Intended Use
This product is used in the "Meijia" automatic biochemical analyzer to quantitatively detect albumin in human serum and plasma.
Product Type (Level 1)
A Clinical chemistry and clinical toxicology
Product Type (Level 2)
A1035 Albumin Test System
Import Information
Imported from abroad
Dates and status
Registration Date
Jan 27, 2014
Expiry Date
Jan 27, 2024
About this record

Access comprehensive regulatory information for “Medica” Albumin Reagent Kit (ALB) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 03bc0f7d3ef0b047dd537676c5686d53 and manufactured by MEDICA CORPORATION. The authorized representative in Taiwan is GRAND MARQUIS CO., LTD..

This page provides complete technical specifications, regulatory compliance details. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.

Free DatabasePowered by Pure Global AI89,000+ Devices