Taiwan FDA registration b54dd24063609791f7144765001999be

E-WEFT Medical Imaging Communication Device (Non-sterilized)

TW: "鈺緯" 醫學影像通訊裝置 (未滅菌)

Taiwan·Risk Class 1·Zhonghe No. 2 Factory of Yuwei Technology Development Co., Ltd·Registered Feb 05, 2024 – Feb 05, 2029Active

Registration details

Analysis ID: b54dd24063609791f7144765001999be

Company information

Manufacturer: Zhonghe No. 2 Factory of Yuwei Technology Development Co., Ltd
Manufacturer Country: Taiwan, Province of China
Authorized Representative: DIVA LABORATORIES, LTD.

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: QMS/QSD;; 國產

Dates and status

Registration Date: Feb 05, 2024
Expiry Date: Feb 05, 2029

About this record

Access comprehensive regulatory information for E-WEFT 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 b54dd24063609791f7144765001999be and manufactured by Zhonghe No. 2 Factory of Yuwei Technology Development Co., Ltd. The authorized representative in Taiwan is DIVA LABORATORIES, LTD..

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