"Simonzi" Anti-Muller's Tube Helmont Detection Team
- Analysis ID
- bc4faf4e4eb5f8b3060408e76b092c7d
- Customs Code
- DHA05603709201
- Manufacturer
- SIEMENS HEALTHCARE DIAGNOSTICS INC.
- Manufacturer Country
- United States
- Authorized Representative
- SIEMENS HEALTHCARE LIMITED
- 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
- Registration Date
- Jul 17, 2024
- Expiry Date
- Jul 17, 2029
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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.