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DLP METAL TIP ARTERIAL CANNULA - FDA Registration 532b9c3e0bd2898a8cfc6416048ab1de

Access comprehensive regulatory information for DLP METAL TIP ARTERIAL CANNULA in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID 532b9c3e0bd2898a8cfc6416048ab1de and manufactured by Viant Medical, Inc. The device was registered on August 01, 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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532b9c3e0bd2898a8cfc6416048ab1de
DLP METAL TIP ARTERIAL CANNULA
FDA ID: 532b9c3e0bd2898a8cfc6416048ab1de
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Device Classification
Brand Name
Medtronic
Registration Information
Analysis ID
532b9c3e0bd2898a8cfc6416048ab1de
Registration Date
August 01, 2022
Manufacturer
Authorized Representative