DuraSealXact Family - FDA Registration 5695a889ad7f61a57e5b2f3c8774acc3
Access comprehensive regulatory information for DuraSealXact Family in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID 5695a889ad7f61a57e5b2f3c8774acc3 and manufactured by Availmed S.A. de C.V.. The device was registered on July 05, 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
5695a889ad7f61a57e5b2f3c8774acc3
DuraSealXact Family
FDA ID: 5695a889ad7f61a57e5b2f3c8774acc3
Device Classification
Brand Name
Integrates
Registration Information
Analysis ID
5695a889ad7f61a57e5b2f3c8774acc3
Registration Date
July 05, 2022
Manufacturer
Authorized Representative

