Peripheral Blood Vessel Interventional Catheter Tube - Vietnam Registration 2403367ĐKLH/BYT-HTTB
Access comprehensive regulatory information for Peripheral Blood Vessel Interventional Catheter Tube in Vietnam's medical device market through Pure Global AI's free database. This Risk Class TTBYT Loại D medical device is registered under number 2403367ĐKLH/BYT-HTTB and manufactured by Goodman Seki Facility. The authorized representative in Vietnam is CÔNG TY TNHH NIPRO SALES VIỆT NAM.
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Device Details
Registration Details
2403367ĐKLH/BYT-HTTB
000.00.04.G18-230329-0028
CROSSROADS MG Guiding shealth
GP60025ST3, GP60050ST3, GP60055ST3, GP60075ST3, GP60045ST3, GP60090ST3
Technical Details
The product is used to guide the catheter to the target lesion in endovascular surgery, including the peripheral blood vessels of the abdomen and the extremities (excluding the brain, spinal cord, and coronary arteries) and is used to deliver various types of drugs, including angiographic contrast agents.
Dates and Status
Nov 06, 2024

