Leica Microsystems-M320 - FDA Registration eca8fa992249559ce6693c0ab81d4bb2
Access comprehensive regulatory information for Leica Microsystems-M320 in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID eca8fa992249559ce6693c0ab81d4bb2 and manufactured by Leica Instruments (Singapore) Pte Ltd. The device was registered on November 05, 2021.
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
eca8fa992249559ce6693c0ab81d4bb2
Leica Microsystems-M320
FDA ID: eca8fa992249559ce6693c0ab81d4bb2
Device Classification
Brand Name
Leica
Registration Information
Analysis ID
eca8fa992249559ce6693c0ab81d4bb2
Registration Date
November 05, 2021
Manufacturer
Authorized Representative

