Taiwan FDA registration bc4faf4e4eb5f8b3060408e76b092c7d

"Simonzi" Anti-Muller's Tube Helmont Detection Team

TW: "西門子" 抗穆勒氏管賀爾蒙檢測試劑組
Taiwan flagTaiwan·Risk Class 2·SIEMENS HEALTHCARE DIAGNOSTICS INC.·Registered Jul 17, 2024 – Jul 17, 2029Active
Registration details
Analysis ID
bc4faf4e4eb5f8b3060408e76b092c7d
Customs Code
DHA05603709201
Company information
Manufacturer Country
United States
Authorized Representative
SIEMENS HEALTHCARE LIMITED
Product details
Intended Use
This product is intended for in vitro diagnostic use and is used with the Atellica IM Analyzer to quantify anti-Mullerian hormone (AMH) in human serum and plasma (lithium heparin).
Product Type (Level 1)
A Clinical chemistry and clinical toxicology
Product Type (Level 2)
A.9999 Miscellaneous  
Import Information
Input;; QMS/QSD
Dates and status
Registration Date
Jul 17, 2024
Expiry Date
Jul 17, 2029
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About this record

Access comprehensive regulatory information for "Simonzi" Anti-Muller's Tube Helmont Detection Team in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number bc4faf4e4eb5f8b3060408e76b092c7d and manufactured by SIEMENS HEALTHCARE DIAGNOSTICS INC.. The authorized representative in Taiwan is SIEMENS HEALTHCARE LIMITED.

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including SIEMENS HEALTHCARE DIAGNOSTICS INC., and 1 recent registrations in the same category. 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.

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