Taiwan FDA registration 597f5ee5557c5d613e92a9e01639010d
Maxjet blood purification circuit catheter
TW: 邁捷血液淨化迴路導管
Taiwan·Risk Class 2·Maxjet Corporation;; Shande Biochemical Technology Co., Ltd. is loyal to the factory·Registered Apr 22, 2009 – Apr 22, 2019CancelledRegistration details
- Analysis ID
- 597f5ee5557c5d613e92a9e01639010d
- Customs Code
- DHY00500268906
Company information
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- Maxjet Corporation
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order.
- Product Type (Level 1)
- H Gastroenterology and urology
- Product Type (Level 2)
- H.5820 血液透析系統及其附件
- Import Information
- Contract manufacturing;; Domestic
Dates and status
- Registration Date
- Apr 22, 2009
- Expiry Date
- Apr 22, 2019
- Cancellation Date
- Jun 17, 2022
Cancellation information
- Status
- Logged out
- Reason
- 自行鍵入;;許可證已逾有效期
About this record
Access comprehensive regulatory information for Maxjet blood purification circuit catheter in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 597f5ee5557c5d613e92a9e01639010d and manufactured by Maxjet Corporation;; Shande Biochemical Technology Co., Ltd. is loyal to the factory. The authorized representative in Taiwan is Maxjet Corporation.
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