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"ABBOTT" ARCHITECT i System (Non-Sterile) - Taiwan Registration 3aab9a1f738d1b911308aa6f53520275

Access comprehensive regulatory information for "ABBOTT" ARCHITECT i System (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 3aab9a1f738d1b911308aa6f53520275 and manufactured by ABBOTT LABORATORIES. 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 ABBOTT LABORATORIES, 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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3aab9a1f738d1b911308aa6f53520275
Registration Details
Taiwan FDA Registration: 3aab9a1f738d1b911308aa6f53520275
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Device Details

"ABBOTT" ARCHITECT i System (Non-Sterile)
TW: "ไบžๅŸน" ่จญ่จˆๅธซ่‡ชๅ‹•ๅ…็–ซๅˆ†ๆžๅ„€ (ๆœชๆป…่Œ)
Risk Class 1
MD
Cancelled

Registration Details

3aab9a1f738d1b911308aa6f53520275

Ministry of Health Medical Device Import No. 019233

DHA09401923308

Company Information

United States

Product Details

A Clinical chemistry and clinical toxicology

A2160 Individual photometric chemistry analyzer for clinical use

Imported from abroad

Dates and Status

Jun 25, 2018

Jun 25, 2023

Cancellation Information

Logged out

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