Taiwan FDA registration 0c60f1c32c1bea4537d9118bd3aded83

"Neo-branched" human immunodeficiency virus antibody Western ink dot method 2.2 test reagent

TW: “新科化” 人類免疫缺乏病毒抗體西方墨點法2.2檢驗試劑
Taiwan flagTaiwan·Risk Class 3·MP BIOMEDICALS ASIA PACIFIC PTE. LTD.·Registered Aug 16, 2012 – Apr 07, 2014Cancelled
Registration details
Analysis ID
0c60f1c32c1bea4537d9118bd3aded83
Customs Code
DHA00602384706
Company information
Manufacturer Country
Singapore
Authorized Representative
NEW SCIENTIFIC EQUIPMENT CO., LTD.
Product details
Intended Use
Western ink dot testing for HIV-1 and HIV-2 antibodies in human serum or plasma can be used as a confirmation reagent for HIV-1, and HIV-2 positive patients should be confirmed with other reagents.
Product Type (Level 1)
B Hematology, pathology, and genetics
Product Type (Level 2)
B.4020 Analysis of specific tests
Import Information
import
Dates and status
Registration Date
Aug 16, 2012
Expiry Date
Apr 07, 2014
Cancellation Date
Nov 15, 2016
Cancellation information
Status
Logged out
Reason
未展延而逾期者
About this record

Access comprehensive regulatory information for "Neo-branched" human immunodeficiency virus antibody Western ink dot method 2.2 test reagent in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number 0c60f1c32c1bea4537d9118bd3aded83 and manufactured by MP BIOMEDICALS ASIA PACIFIC PTE. LTD.. The authorized representative in Taiwan is NEW SCIENTIFIC EQUIPMENT CO., LTD..

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