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ABBOTT ARCHITECT DHEA-S (Non-Sterile) - Taiwan Registration 2a48b5b65b6adbb9e11b235994b40b14

Access comprehensive regulatory information for ABBOTT ARCHITECT DHEA-S (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 2a48b5b65b6adbb9e11b235994b40b14 and manufactured by BIOKIT S.A.. The authorized representative in Taiwan is ABBOTT LABORATORIES SERVICES LLC TAIWAN BRANCH (U.S.A.).

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including BIOKIT S.A., 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.

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2a48b5b65b6adbb9e11b235994b40b14
Registration Details
Taiwan FDA Registration: 2a48b5b65b6adbb9e11b235994b40b14
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Device Details

ABBOTT ARCHITECT DHEA-S (Non-Sterile)
TW: ไบžๅŸน่จญ่จˆๅธซ่„ซๆฐซ็•ฐ้›„ๅ›บ้…ฎ็กซ้…ธ้นฝๆชข้ฉ—่ฉฆๅŠ‘็ต„(ๆœชๆป…่Œ)
Risk Class 1
MD

Registration Details

2a48b5b65b6adbb9e11b235994b40b14

Ministry of Health Medical Device Import No. 019713

DHA09401971309

Company Information

Product Details

Limited to the first level identification range of the Measures for the Administration of Medical Devices "Dehydroepiandrosterone (Free and Sulfur Salts) Test System (A.1245)".

A Clinical chemistry and clinical toxicology

A1245 Dehydroepiandrosterone (Free and Sulfur) Test System

Imported from abroad

Dates and Status

Oct 18, 2018

Oct 18, 2023

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