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L-ANEURYSM-CLIP® SYSTEM - FDA Registration ea504a2ff2c33536d618217fdc839e14

Access comprehensive regulatory information for L-ANEURYSM-CLIP® SYSTEM in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID ea504a2ff2c33536d618217fdc839e14 and manufactured by Peter Lazic GmbH. The device was registered on May 24, 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
ea504a2ff2c33536d618217fdc839e14
L-ANEURYSM-CLIP® SYSTEM
FDA ID: ea504a2ff2c33536d618217fdc839e14
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Device Classification
Brand Name
Peter Lazic
Registration Information
Analysis ID
ea504a2ff2c33536d618217fdc839e14
Registration Date
May 24, 2022
Manufacturer
Authorized Representative