Taiwan FDA registration d6cbeba8dc99dae15231adb1f9b5575e

"Antu" Intensive Medium (Sterilized)

TW: "安圖" 強化培養基(滅菌)

Taiwan·Risk Class 1·Autobio Diagnostics Co., Ltd.·Registered Mar 01, 2024 – Mar 01, 2029Active

Registration details

Analysis ID: d6cbeba8dc99dae15231adb1f9b5575e
Customs Code: DHA09600489500

Company information

Manufacturer: Autobio Diagnostics Co., Ltd.
Manufacturer Country: China
Authorized Representative: DiaTech Technology Co., Ltd.

Product details

Intended Use: 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.
Product Type (Level 1): C Immunology and microbiology
Product Type (Level 2): C.2330 Enhanced culture medium
Import Information: QMS/QSD;; Chinese goods;; input

Dates and status

Registration Date: Mar 01, 2024
Expiry Date: Mar 01, 2029

About this record

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.