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IL ACL Elite Pro - Taiwan Registration 7fd35d6105cf2b2a356ef7cfd3aa0d0e

Access comprehensive regulatory information for IL ACL Elite Pro in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 7fd35d6105cf2b2a356ef7cfd3aa0d0e and manufactured by INSTRUMENTATION LABORATORY CO.. The authorized representative in Taiwan is Werfen Taiwan Limited.

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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7fd35d6105cf2b2a356ef7cfd3aa0d0e
Registration Details
Taiwan FDA Registration: 7fd35d6105cf2b2a356ef7cfd3aa0d0e
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Device Details

IL ACL Elite Pro
TW: ๅฏฆ้ฉ—ๅ„€ๅ™จๅ…ฌๅธๅ…จ่‡ชๅ‹•ๅ‡่ก€ๅˆ†ๆžๅ„€
Risk Class 2
MD

Registration Details

7fd35d6105cf2b2a356ef7cfd3aa0d0e

Ministry of Health Medical Device Import No. 029816

DHA05602981605

Company Information

United States

Product Details

This product is an automatic analysis system for blood coagulation test and fibrinolysis test.

B Hematology and pathology devices

B5425 Multifunctional equipment for in vitro agglutination research

Imported from abroad

Dates and Status

Aug 04, 2017

Aug 04, 2027