Malaysia MDA registration GD4410624-160231

CORDIS MAXI LD® LARGE DIAMETER BALLOON PERCUTANEOUS TRANSLUMINAL ANGIOPLASTY (PTA) DILATATION CATHETER

Malaysia·D·CORDIS·Valid January 19, 2024 – January 18, 2029Active

Device classification

Risk Class: D
Brand Name: CORDIS

Registration information

Analysis ID: GD4410624-160231
Registration Date: January 19, 2024
Expiration Date: January 18, 2029

Authorized Representative

Name: INSAN DAMAI SDN BHD

About this record

Access comprehensive regulatory information for CORDIS MAXI LD® LARGE DIAMETER BALLOON PERCUTANEOUS TRANSLUMINAL ANGIOPLASTY (PTA) DILATATION CATHETER in the Malaysia medical device market through Pure Global AI's free database. This D medical device is registered under MDA ID GD4410624-160231 with brand name CORDIS. The device was registered on January 19, 2024.

This page provides complete registration details including authorized representative details, brand information, and regulatory compliance data from the official Malaysia MDA medical device database. Pure Global AI offers free access to Malaysia's complete medical device registry.