Quintus™ 5-Part Stopper - FDA Registration 880a97d34e59b9f7955527419e095265
Access comprehensive regulatory information for Quintus™ 5-Part Stopper in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID 880a97d34e59b9f7955527419e095265 and manufactured by Clinical Diagnostic Solutions, Inc.. The device was registered on December 16, 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
880a97d34e59b9f7955527419e095265
Quintus™ 5-Part Stopper
FDA ID: 880a97d34e59b9f7955527419e095265
Device Classification
Brand Name
Quintus
Registration Information
Analysis ID
880a97d34e59b9f7955527419e095265
Registration Date
December 16, 2022
Manufacturer
Authorized Representative

