Taiwan FDA registration e99b83356201cb66e1f28f9ed96434b7
"Mindray" automatic external defibrillator and accessories
TW: “邁瑞”自動體外去顫器及配件
Taiwan·Risk Class 3·Shenzhen Mindray Bio-Medical Electronics Co., Ltd.·Registered Apr 16, 2020 – Apr 16, 2025ExpiredRegistration details
- Analysis ID
- e99b83356201cb66e1f28f9ed96434b7
- Customs Code
- DHA09200113103
Company information
- Manufacturer Country
- China
- Authorized Representative
- Medone Medical Equipment Co., Ltd.
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- E Cardiovascular Medicine Science
- Product Type (Level 2)
- E.5310 自動體外去顫器系統
- Import Information
- Chinese goods;; input
Dates and status
- Registration Date
- Apr 16, 2020
- Expiry Date
- Apr 16, 2025
About this record
Access comprehensive regulatory information for "Mindray" automatic external defibrillator and accessories in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number e99b83356201cb66e1f28f9ed96434b7 and manufactured by Shenzhen Mindray Bio-Medical Electronics Co., Ltd.. The authorized representative in Taiwan is Medone Medical Equipment Co., Ltd..
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