Taiwan FDA registration ddcfe236a010cf021586bc7e6a2b7e60
"Lily" disposable sterile central venous catheter group
TW: “百合”一次性無菌中心靜脈導管組
Taiwan·Risk Class 2·GUANGDONG BAIHE MEDICAL TECHNOLOGY CO., LTD.·Registered Jan 06, 2015 – Jan 06, 2020CancelledRegistration details
- Analysis ID
- ddcfe236a010cf021586bc7e6a2b7e60
- Customs Code
- DHA09200064200
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)
- J General hospital and personal use equipment
- Product Type (Level 2)
- J.5200 Endovascular catheters
- Import Information
- Input;; Chinese goods
Dates and status
- Registration Date
- Jan 06, 2015
- Expiry Date
- Jan 06, 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" disposable sterile central venous catheter group in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number ddcfe236a010cf021586bc7e6a2b7e60 and manufactured by GUANGDONG BAIHE MEDICAL TECHNOLOGY CO., LTD.. The authorized representative in Taiwan is HURRAYBIO CO., LTD..
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