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VITEK 2 Gram Positive AST for Fusidic Acid - Taiwan Registration ccb1ca2d394c4fa5de9cfbb6c2627934

Access comprehensive regulatory information for VITEK 2 Gram Positive AST for Fusidic Acid in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number ccb1ca2d394c4fa5de9cfbb6c2627934 and manufactured by bioMรฉrieux, Inc.. The authorized representative in Taiwan is Hong Kong Commercial Mรฉrieux S.p.A. Taiwan Branch.

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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ccb1ca2d394c4fa5de9cfbb6c2627934
Registration Details
Taiwan FDA Registration: ccb1ca2d394c4fa5de9cfbb6c2627934
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Device Details

VITEK 2 Gram Positive AST for Fusidic Acid
TW: ๅพฎ้ตๅ…‹2้ฉ่˜ญๆฐ้™ฝๆ€ง่Œ่—ฅๆ•ๅกๆŠ—็”Ÿ็ด -่ค้ปด็ด 
Risk Class 2
MD

Registration Details

ccb1ca2d394c4fa5de9cfbb6c2627934

Ministry of Health Medical Device Import No. 031414

DHA05603141403

Company Information

United States

Product Details

This product is equipped with Microtek 2 automatic microbial analyzer to determine the antibiotic susceptibility of staphylococci and enterococci in vitro.

C Immunology and microbiology devices

C1645 Automatic Short Incubation Period Antibiotic Susceptibility Testing System

Imported from abroad

Dates and Status

Aug 15, 2018

Aug 15, 2028