Taiwan FDA registration 5b63d46074be4a048555a4647095ddf9
"Huawei" ECG application software
TW: “華為” 心電圖應用軟體
Registration details
- Analysis ID
- 5b63d46074be4a048555a4647095ddf9
- Customs Code
- DHA09200150301
Company information
- Manufacturer
- Huawei Device Co., Ltd.
- Manufacturer Country
- China
- Authorized Representative
- FRONTIER BIO-MEDICAL INC.
Product details
- Intended Use
- Details are as detailed as approved Chinese instructions
- Product Type (Level 1)
- E Cardiovascular Medicine Science
- Product Type (Level 2)
- E.2340 Telecardiogram
- Import Information
- Chinese goods;; input
Dates and status
- Registration Date
- Oct 14, 2023
- Expiry Date
- Oct 14, 2028
About this record
Access comprehensive regulatory information for "Huawei" ECG application software in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 5b63d46074be4a048555a4647095ddf9 and manufactured by Huawei Device Co., Ltd.. The authorized representative in Taiwan is FRONTIER BIO-MEDICAL INC..
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