Taiwan FDA registration a9e4d07d9efe0eb3b94ef7186e4b2b5e

Ampere hepatitis C virus antibody Western ink dot method third-generation test reagent set

TW: 安培C型肝炎病毒抗體西方墨點法第三代檢驗試劑組
Taiwan flagTaiwan·Risk Class 3·MP BIOMEDICALS ASIA PACIFIC PTE. LTD.·Registered Mar 23, 2015 – Mar 23, 2030Active
Registration details
Analysis ID
a9e4d07d9efe0eb3b94ef7186e4b2b5e
Customs Code
DHA05602718308
Company information
Manufacturer Country
Singapore
Product details
Intended Use
This product uses enzyme immunoassay to qualitatively detect hepatitis C virus antibodies in human serum and plasma. This product is not approved for blood donor screening.
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
Mar 23, 2015
Expiry Date
Mar 23, 2030
About this record

Access comprehensive regulatory information for Ampere hepatitis C virus antibody Western ink dot method third-generation test reagent set in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number a9e4d07d9efe0eb3b94ef7186e4b2b5e and manufactured by MP BIOMEDICALS ASIA PACIFIC PTE. LTD.. The authorized representative in Taiwan is ABBOTT LABORATORIES SERVICES LLC TAIWAN BRANCH (U.S.A.).

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