Taiwan FDA registration c3922d7dcd68b3c1a73f8b8d8f66d54d

Beckman Coulter Arthurs Anti-Muller's Hormone Correction Fluid/Tube Fluid

TW: 貝克曼庫爾特亞瑟斯抗穆勒氏荷爾蒙校正液/品管液
Taiwan flagTaiwan·Risk Class 2·IMMUNOTECH SAS, A BECKMAN COULTER COMPANY·Registered Jul 21, 2015 – Jul 21, 2025Expired
Registration details
Analysis ID
c3922d7dcd68b3c1a73f8b8d8f66d54d
Customs Code
DHA05602752306
Company information
Manufacturer Country
France
Product details
Intended Use
Changed performance to: This product calibrates and monitors Access AMH and Access AMH Advance analysis systems to quantitatively detect the amount of anti-Mullerian hormone in human serum and plasma.
Product Type (Level 1)
A Clinical chemistry and clinical toxicology
Product Type (Level 2)
A.1150 calibration;; A.1660 Quality control materials (analytical and non-analytical)
Import Information
import
Dates and status
Registration Date
Jul 21, 2015
Expiry Date
Jul 21, 2025
About this record

Access comprehensive regulatory information for Beckman Coulter Arthurs Anti-Muller's Hormone Correction Fluid/Tube Fluid in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number c3922d7dcd68b3c1a73f8b8d8f66d54d and manufactured by IMMUNOTECH SAS, A BECKMAN COULTER COMPANY. The authorized representative in Taiwan is BECKMAN COULTER TAIWAN INC., TAIWAN BRANCH (U.S.A.).

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