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"Antu" Intensive Medium (Sterilized) - Taiwan Registration d6cbeba8dc99dae15231adb1f9b5575e

Access comprehensive regulatory information for "Antu" Intensive Medium (Sterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number d6cbeba8dc99dae15231adb1f9b5575e 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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d6cbeba8dc99dae15231adb1f9b5575e
Registration Details
Taiwan FDA Registration: d6cbeba8dc99dae15231adb1f9b5575e
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Device Details

"Antu" Intensive Medium (Sterilized)
TW: "ๅฎ‰ๅœ–" ๅผทๅŒ–ๅŸน้คŠๅŸบ(ๆป…่Œ)
Risk Class 1

Registration Details

d6cbeba8dc99dae15231adb1f9b5575e

DHA09600489500

Company Information

Product Details

Limited to the first level identification range of the "Intensive Medium (C.2330)" of the Measures for the Classification and Grading Management of Medical Devices.

C Immunology and microbiology

C.2330 Enhanced culture medium

QMS/QSD;; Chinese goods;; input

Dates and Status

Mar 01, 2024

Mar 01, 2029