Taiwan FDA registration c2f7e52cf06483554cbf95ceb330fe9e

"Antu" selective medium (sterilized)

TW: "安圖" 選擇性培養基(滅菌)

Taiwan·Risk Class 1·Autobio Diagnostics Co., Ltd.·Registered Feb 22, 2024 – Feb 22, 2029Active

Registration details

Analysis ID: c2f7e52cf06483554cbf95ceb330fe9e
Customs Code: DHA09600489003

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 of medical devices "Selective culture medium (C.2360)" first level identification range.
Product Type (Level 1): C Immunology and microbiology
Product Type (Level 2): C.2360 選擇性培養基
Import Information: QMS/QSD;; Chinese goods;; input

Dates and status

Registration Date: Feb 22, 2024
Expiry Date: Feb 22, 2029

About this record

Access comprehensive regulatory information for "Antu" selective 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 c2f7e52cf06483554cbf95ceb330fe9e and manufactured by Autobio Diagnostics Co., Ltd.. The authorized representative in Taiwan is DiaTech Technology Co., Ltd..

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