Taiwan FDA registration 94367e128f4adb6cd9f53fd037ca743b

"BenQ" Medical Imaging Communication Device (Non-sterilized)

TW: "明基" 醫學影像通訊裝置 (未滅菌)

Taiwan·Risk Class 1·AUO (Suzhou) Co., Ltd.;; Meiki Dentsu Co., Ltd.·Registered May 20, 2024 – May 20, 2029Active

Registration details

Analysis ID: 94367e128f4adb6cd9f53fd037ca743b
Customs Code: DHA09600494604

Company information

Manufacturer: AUO (Suzhou) Co., Ltd.;; Meiki Dentsu Co., Ltd.
Manufacturer Country: Taiwan, Province of China;;China
Authorized Representative: BENQ CORPORATION

Product details

Intended Use: It is limited to the scope of first-level identification of medical imaging communication devices (P.2020) in the Measures for the Classification and Grading of Medical Devices.
Product Type (Level 1): P Radiology Science
Product Type (Level 2): P.2020 Medical imaging communication devices
Import Information: Input;; QMS/QSD;; Contract manufacturing;; Chinese goods

Dates and status

Registration Date: May 20, 2024
Expiry Date: May 20, 2029

About this record

Access comprehensive regulatory information for "BenQ" Medical Imaging Communication Device (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 94367e128f4adb6cd9f53fd037ca743b and manufactured by AUO (Suzhou) Co., Ltd.;; Meiki Dentsu Co., Ltd.. The authorized representative in Taiwan is BENQ CORPORATION.

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