Taiwan FDA registration de02bbc3fef493e960139b5d7338ee51
"Mindray" infusion pump
TW: ＂邁瑞＂輸液幫浦
Taiwan·Risk Class 2·Shenzhen Mindray Bio-Medical Electronics Co., Ltd.;; Shenzhen Mindray Scientific Co., Ltd.·Registered May 26, 2022 – May 26, 2027ActiveRegistration details
- Analysis ID
- de02bbc3fef493e960139b5d7338ee51
- Customs Code
- DHA09200133802
Company information
- Manufacturer
- Shenzhen Mindray Bio-Medical Electronics Co., Ltd.;; Shenzhen Mindray Scientific Co., Ltd.
- Manufacturer Country
- China
- Authorized Representative
- TAIWAN MEDICAL SERVICES CORPORATION
Product details
- Intended Use
- Details are as detailed as approved Chinese instructions
- Product Type (Level 1)
- J General hospital and personal use equipment
- Product Type (Level 2)
- J.5725 Infusion 幫浦
- Import Information
- Chinese goods;; input
Dates and status
- Registration Date
- May 26, 2022
- Expiry Date
- May 26, 2027
About this record
Access comprehensive regulatory information for "Mindray" infusion pump in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number de02bbc3fef493e960139b5d7338ee51 and manufactured by Shenzhen Mindray Bio-Medical Electronics Co., Ltd.;; Shenzhen Mindray Scientific Co., Ltd.. The authorized representative in Taiwan is TAIWAN MEDICAL SERVICES CORPORATION.
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