Taiwan FDA registration fe96e956d063cb2566dbacb298840073

"Antu" Identification Medium (Sterilized)

TW: "安圖" 鑑別培養基 (滅菌)

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

Registration details

Analysis ID: fe96e956d063cb2566dbacb298840073
Customs Code: DHA09600489602

Company information

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

Product details

Intended Use: Limited to the classification and grading management measures of medical equipment "Identification medium (C.2320)The first level identification range.
Product Type (Level 1): C Immunology and microbiology
Product Type (Level 2): C.2320 Differential culture media
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" Identification 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 fe96e956d063cb2566dbacb298840073 and manufactured by Autobio Diagnostics Co., Ltd.. The authorized representative in Taiwan is DiaTech Technology Co., Ltd..

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