"Siemens" blood ammonia test reagent (unsterilized) - Taiwan Registration e02fd692878ac3ce160b49906906329b
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 e02fd692878ac3ce160b49906906329b and manufactured by SIEMENS HEALTHCARE DIAGNOSTICS INC.;; RANDOX LABORATORIES LTD.. The authorized representative in Taiwan is SIEMENS HEALTHCARE LIMITED.
This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including SEKISUI DIAGNOSTICS P.E.I. 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.
Device Details
Registration Details
e02fd692878ac3ce160b49906906329b
DHA04400586704
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
import
Dates and Status
May 21, 2007
May 21, 2027