Taiwan FDA registration 6f8b685a374e30a795199b27c406c553
"Lily" single-use sterile hemodialysis catheters and accessories
TW: “百合”一次性使用無菌血液透析導管及附件
Taiwan·Risk Class 2·Guangdong Baihe Medical Technology Co., Ltd.·Registered Jan 30, 2015 – Jan 30, 2020CancelledRegistration details
- Analysis ID
- 6f8b685a374e30a795199b27c406c553
- Customs Code
- DHA09200067502
Company information
- Manufacturer
- Guangdong Baihe Medical Technology Co., Ltd.
- Manufacturer Country
- China
- Authorized Representative
- HURRAYBIO CO., LTD.
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
- Chinese goods;; input
Dates and status
- Registration Date
- Jan 30, 2015
- Expiry Date
- Jan 30, 2020
- Cancellation Date
- May 19, 2022
Cancellation information
- Status
- Logged out
- Reason
- 自行鍵入
About this record
Access comprehensive regulatory information for "Lily" single-use sterile hemodialysis catheters and accessories in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 6f8b685a374e30a795199b27c406c553 and manufactured by Guangdong Baihe Medical Technology Co., Ltd.. The authorized representative in Taiwan is HURRAYBIO CO., LTD..
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