Vietnam MOH registration 2403367ĐKLH/BYT-HTTB

Peripheral Blood Vessel Interventional Catheter Tube

VN: Ống thông can thiệp mạch máu ngoại vi
Vietnam flagVietnam·Risk Class TTBYT Loại D·CROSSROADS MG Guiding shealth·Goodman Seki Facility·Registered Nov 06, 2024
Registration details
Analysis ID
2403367ĐKLH/BYT-HTTB
Submission ID
000.00.04.G18-230329-0028
Product Type
CROSSROADS MG Guiding shealth
Product Code
GP60025ST3, GP60050ST3, GP60055ST3, GP60075ST3, GP60045ST3, GP60090ST3
Company information
Manufacturer Country
JAPAN
Product Owner
Goodman Co.,Ltd,
Authorized Representative
CÔNG TY TNHH NIPRO SALES VIỆT NAM
Technical details
Intended Use
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
Registration Date
Nov 06, 2024
About this record

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.

Free DatabasePowered by Pure Global AI300,000+ Devices