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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.

This page provides complete technical specifications, regulatory compliance details. Pure Global AI offers free access to 300,000+ Vietnamese medical device registrations, helping global MedTech companies navigate Vietnam MOH regulations, identify competitors, and discover partnership opportunities efficiently.

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2403367ĐKLH/BYT-HTTB
Registration Details
Vietnam MOH Registration: 2403367ĐKLH/BYT-HTTB
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Device Details

Peripheral Blood Vessel Interventional Catheter Tube
VN: Ống thông can thiệp mạch máu ngoại vi
Risk Class TTBYT Loại D

Registration Details

2403367ĐKLH/BYT-HTTB

000.00.04.G18-230329-0028

CROSSROADS MG Guiding shealth

GP60025ST3, GP60050ST3, GP60055ST3, GP60075ST3, GP60045ST3, GP60090ST3

Company Information

JAPAN

Goodman Co.,Ltd,

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