Taiwan FDA registration 91baf6c95e59d41cc02ad25b070f3ecc

"Antu" automatic blood culture apparatus (non-sterilized)

TW: "安圖" 全自動血液培養儀 (未滅菌)

Taiwan·Risk Class 1·Autobio Labtec Instruments Co., Ltd.·Registered Jan 18, 2024 – Jan 18, 2029Active

Registration details

Analysis ID: 91baf6c95e59d41cc02ad25b070f3ecc
Customs Code: DHA09600487102

Company information

Manufacturer: Autobio Labtec Instruments 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: Chinese goods;; Input;; QMS/QSD

Dates and status

Registration Date: Jan 18, 2024
Expiry Date: Jan 18, 2029

About this record

Access comprehensive regulatory information for "Antu" automatic blood culture apparatus (non-sterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 91baf6c95e59d41cc02ad25b070f3ecc and manufactured by Autobio Labtec Instruments Co., Ltd.. The authorized representative in Taiwan is DiaTech Technology Co., Ltd..

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