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"Siemens" thyroglobulin autologous antibody reagent - Taiwan Registration 297c33d57973ddac3d63d90eaa7a8e41

Access comprehensive regulatory information for "Siemens" thyroglobulin autologous antibody reagent in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 297c33d57973ddac3d63d90eaa7a8e41 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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297c33d57973ddac3d63d90eaa7a8e41
Registration Details
Taiwan FDA Registration: 297c33d57973ddac3d63d90eaa7a8e41
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Device Details

"Siemens" thyroglobulin autologous antibody reagent
TW: "่ฅฟ้–€ๅญ" ็”ฒ็‹€่…บ็ƒ่›‹็™ฝ่‡ช้ซ”ๆŠ—้ซ”่ฉฆๅŠ‘็ต„
Risk Class 2

Registration Details

297c33d57973ddac3d63d90eaa7a8e41

DHA00601515800

Company Information

United States

Product Details

This product is suitable for ADVIA Centaur, ADVIA Centaur XP, ADVIA Centaur CP analyzer to quantitatively determine the concentration of thyroglobulin autoantibodies in serum or EDTA-containing plasma.

C Immunology and microbiology

import

Dates and Status

Dec 01, 2005

Dec 01, 2025

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