Taiwan FDA registration bd4a3c434241243fc069e8baf1850434
"Jiayang" ureters
TW: “佳洋”導尿管
Taiwan·Risk Class 2·URO TECHNOLOGY SDN BHD·Registered Sep 09, 2011 – Sep 09, 2021CancelledRegistration details
- Analysis ID
- bd4a3c434241243fc069e8baf1850434
- Customs Code
- DHA00602278607
Company information
- Manufacturer
- URO TECHNOLOGY SDN BHD
- Manufacturer Country
- Malaysia
- Authorized Representative
- ANDERSON MEDICARE 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.5130 泌尿導管及其附件
- Import Information
- import
Dates and status
- Registration Date
- Sep 09, 2011
- Expiry Date
- Sep 09, 2021
- Cancellation Date
- Oct 12, 2023
Cancellation information
- Status
- Logged out
- Reason
- 未展延而逾期者
About this record
Access comprehensive regulatory information for "Jiayang" ureters in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number bd4a3c434241243fc069e8baf1850434 and manufactured by URO TECHNOLOGY SDN BHD. The authorized representative in Taiwan is ANDERSON MEDICARE CO., LTD..
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