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Abbott Designer Dehydroepiandrosterone (Sulfur Salt) Test Set - Taiwan Registration 5d53204b476f11e2cbf5be1dd0dd1b7f

Access comprehensive regulatory information for Abbott Designer Dehydroepiandrosterone (Sulfur Salt) Test Set in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 5d53204b476f11e2cbf5be1dd0dd1b7f and manufactured by ABBOTT GMBH & CO. Medical history. The authorized representative in Taiwan is ABBOTT LABORATORIES SERVICES LLC 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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5d53204b476f11e2cbf5be1dd0dd1b7f
Registration Details
Taiwan FDA Registration: 5d53204b476f11e2cbf5be1dd0dd1b7f
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Device Details

Abbott Designer Dehydroepiandrosterone (Sulfur Salt) Test Set
TW: ไบžๅŸน่จญ่จˆๅธซๅŽปๆฐซ่กจ้›„ๅ›บ้…ฎ(็กซ้นฝ)ๆชข้ฉ—่ฉฆๅŠ‘็ต„
Risk Class 1
Cancelled

Registration Details

5d53204b476f11e2cbf5be1dd0dd1b7f

DHA04400451507

Company Information

Product Details

A Clinical chemistry and clinical toxicology

A.1245 Dehydroepiandrosterone (Free and Sulfur Salt) Test System

import

Dates and Status

May 18, 2006

May 18, 2011

Nov 06, 2012

Cancellation Information

Logged out

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