"Siemens" blood ammonia test reagent (unsterilized) - Taiwan Registration 8ac3a76c2b5beeca27173f87a414964a
Access comprehensive regulatory information for "Siemens" blood ammonia test reagent (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 8ac3a76c2b5beeca27173f87a414964a and manufactured by SEKISUI DIAGNOSTICS P.E.I. 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.;; RANDOX LABORATORIES LTD., 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.
Device Details
Product Details
It is limited to the first-level identification scope of the "Blood Ammonia Test System (A.1065)" of the Measures for the Classification and Grading of Medical Devices.
A Clinical chemistry and clinical toxicology
A.1065 ่กๆฐจ่ฉฆ้ฉ็ณป็ตฑ
QMS/QSD;; ่ผธๅ ฅ
Dates and Status
Oct 14, 2019
Oct 14, 2029