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Beckman Coulter Insulin Reagent Set (non-sterile) - Taiwan Registration 7f4b4ca60e336c8d6884ae15fd66367f

Access comprehensive regulatory information for Beckman Coulter Insulin Reagent Set (non-sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 7f4b4ca60e336c8d6884ae15fd66367f and manufactured by BECKMAN COULTER, INC.. The authorized representative in Taiwan is BECKMAN COULTER TAIWAN INC., TAIWAN BRANCH (U.S.A.).

This page provides complete technical specifications, regulatory compliance details. 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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7f4b4ca60e336c8d6884ae15fd66367f
Registration Details
Taiwan FDA Registration: 7f4b4ca60e336c8d6884ae15fd66367f
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Device Details

Beckman Coulter Insulin Reagent Set (non-sterile)
TW: ่ฒๅ…‹ๆ›ผๅบซ็ˆพ็‰น่ƒฐๅณถ็ด ่ฉฆๅŠ‘็ต„(ๆœชๆป…่Œ)
Risk Class 1

Registration Details

7f4b4ca60e336c8d6884ae15fd66367f

DHA09402365803

Company Information

United States

Product Details

It is limited to the first level of identification of the immune response insulin test system (A.1405) of the classification and grading management measures for medical devices.

A Clinical chemistry and clinical toxicology

A.1405 Immune Response Insulin Test System

Input;; QMS/QSD

Dates and Status

Nov 04, 2024

Nov 04, 2029