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Abbott ICE Syphilis - Taiwan Registration e7988601d83ce49bf5e0fd0315ef2cd1

Access comprehensive regulatory information for Abbott ICE Syphilis in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number e7988601d83ce49bf5e0fd0315ef2cd1 and manufactured by DIASORIN S.P.A. UK BRANCH. 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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e7988601d83ce49bf5e0fd0315ef2cd1
Registration Details
Taiwan FDA Registration: e7988601d83ce49bf5e0fd0315ef2cd1
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Device Details

Abbott ICE Syphilis
TW: ไบžๅŸนๆข…ๆฏ’่žบๆ—‹้ซ”่ฉฆๅŠ‘็ต„
Risk Class 2
MD
Cancelled

Registration Details

e7988601d83ce49bf5e0fd0315ef2cd1

Ministry of Health Medical Device Import No. 031119

DHA05603111901

Company Information

Product Details

C Immunology and microbiology devices

C3830 Treponema pallidum reagent

Imported from abroad

Dates and Status

May 25, 2018

May 25, 2023

May 12, 2023

Cancellation Information

Logged out

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