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"Antu" Bixi Series Blood Cultivation Base (Bactericidal) - Taiwan Registration 1c1ac9c915d5cbf1f4841f33b9f9ff03

Access comprehensive regulatory information for "Antu" Bixi Series Blood Cultivation Base (Bactericidal) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 1c1ac9c915d5cbf1f4841f33b9f9ff03 and manufactured by Autobio Diagnostics Co., Ltd.. The authorized representative in Taiwan is DiaTech Technology Co., Ltd..

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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1c1ac9c915d5cbf1f4841f33b9f9ff03
Registration Details
Taiwan FDA Registration: 1c1ac9c915d5cbf1f4841f33b9f9ff03
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Device Details

"Antu" Bixi Series Blood Cultivation Base (Bactericidal)
TW: "ๅฎ‰ๅœ–" ๅฟ…ๅ–œ็ณปๅˆ—่ก€ๆถฒๅŸน้คŠๅŸบ (ๆป…่Œ)
Risk Class 1

Registration Details

1c1ac9c915d5cbf1f4841f33b9f9ff03

DHA09600492101

Company Information

Product Details

It is limited to the first level of identification scope of the microbial growth monitor (C.2560) of the management measures for the classification and grading of medical devices.

C Immunology and microbiology

C.2560 Microbial growth monitors

QMS/QSD;; Chinese goods;; input

Dates and Status

Apr 02, 2024

Apr 02, 2029