Double Lumen Catheter Set - FDA Registration f42d76b8536645ffe50a7f285b7a4011
Access comprehensive regulatory information for Double Lumen Catheter Set in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID f42d76b8536645ffe50a7f285b7a4011 and manufactured by MARTECH MEDICAL PRODUCTS S.DE RL. DE CV. The device was registered on March 25, 2022.
This page provides complete registration details including manufacturer information, authorized representative details, and regulatory compliance data from the official Myanmar FDA medical device database. Pure Global AI offers free access to Myanmar's complete medical device registry.
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FDA Official Data
f42d76b8536645ffe50a7f285b7a4011
Double Lumen Catheter Set
FDA ID: f42d76b8536645ffe50a7f285b7a4011
Device Classification
Brand Name
Nipro
Registration Information
Analysis ID
f42d76b8536645ffe50a7f285b7a4011
Registration Date
March 25, 2022
Manufacturer
Authorized Representative

