Taiwan FDA registration a3973e4bfcfbc8dce27bb1f564bd28d5
"Ketu" blood circuit tube group
TW: “凱圖”血液迴路管組
Taiwan·Risk Class 2·Jiacheng Seiko Co., Ltd. second factory·Registered Apr 19, 2016 – Apr 11, 2018CancelledRegistration details
- Analysis ID
- a3973e4bfcfbc8dce27bb1f564bd28d5
Company information
- Manufacturer
- Jiacheng Seiko Co., Ltd. second factory
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- K2 INTERNATIONAL MEDICAL INC.
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.5540 Blood Access Devices and Accessories
- Import Information
- Contract manufacturing;; Domestic
Dates and status
- Registration Date
- Apr 19, 2016
- Expiry Date
- Apr 11, 2018
- Cancellation Date
- Dec 20, 2019
Cancellation information
- Status
- Logged out
- Reason
- 未展延而逾期者
About this record
Access comprehensive regulatory information for "Ketu" blood circuit tube group in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number a3973e4bfcfbc8dce27bb1f564bd28d5 and manufactured by Jiacheng Seiko Co., Ltd. second factory. The authorized representative in Taiwan is K2 INTERNATIONAL MEDICAL INC..
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