Taiwan FDA registration 1c1ac9c915d5cbf1f4841f33b9f9ff03

"Antu" Bixi Series Blood Cultivation Base (Bactericidal)

TW: "安圖" 必喜系列血液培養基 (滅菌)

Taiwan·Risk Class 1·Autobio Diagnostics Co., Ltd.·Registered Apr 02, 2024 – Apr 02, 2029Active

Registration details

Analysis ID: 1c1ac9c915d5cbf1f4841f33b9f9ff03
Customs Code: DHA09600492101

Company information

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

Product details

Intended Use: 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.
Product Type (Level 1): C Immunology and microbiology
Product Type (Level 2): C.2560 Microbial growth monitors
Import Information: QMS/QSD;; Chinese goods;; input

Dates and status

Registration Date: Apr 02, 2024
Expiry Date: Apr 02, 2029

About this record

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..

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