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Beckman Coulter Human Growth Hormone Reagent Set (non-sterile) - Taiwan Registration a0d2be1b70f652ea38007be6ce779045

Access comprehensive regulatory information for Beckman Coulter Human Growth Hormone 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 a0d2be1b70f652ea38007be6ce779045 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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a0d2be1b70f652ea38007be6ce779045
Registration Details
Taiwan FDA Registration: a0d2be1b70f652ea38007be6ce779045
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Device Details

Beckman Coulter Human Growth Hormone Reagent Set (non-sterile)
TW: ่ฒๅ…‹ๆ›ผๅบซ็ˆพ็‰นไบบ้กž็”Ÿ้•ทๆฟ€็ด ่ฉฆๅŠ‘็ต„(ๆœชๆป…่Œ)
Risk Class 1

Registration Details

a0d2be1b70f652ea38007be6ce779045

DHA09402360001

Company Information

United States

Product Details

It is limited to the first level of identification of the human growth hormone test system (A.1370) of the classification and grading management measures for medical devices.

A Clinical chemistry and clinical toxicology

A.1370 Human Growth Hormone Testing System

QMS/QSD;; ่ผธๅ…ฅ

Dates and Status

Sep 10, 2024

Sep 10, 2029