CORDIS MAXI LD® LARGE DIAMETER BALLOON PERCUTANEOUS TRANSLUMINAL ANGIOPLASTY (PTA) DILATATION CATHETER - MDA Registration GD4410624-160231
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.
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D
GD4410624-160231
CORDIS MAXI LD® LARGE DIAMETER BALLOON PERCUTANEOUS TRANSLUMINAL ANGIOPLASTY (PTA) DILATATION CATHETER
MDA ID: GD4410624-160231
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

