Leica Microsystems-M822 - FDA Registration 0ad962ec38dd14a782b15129df09c5ad
Access comprehensive regulatory information for Leica Microsystems-M822 in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID 0ad962ec38dd14a782b15129df09c5ad and manufactured by Leica Instruments (Singapore) Pte Ltd. The device was registered on April 07, 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
0ad962ec38dd14a782b15129df09c5ad
Leica Microsystems-M822
FDA ID: 0ad962ec38dd14a782b15129df09c5ad
Device Classification
Brand Name
Leica
Registration Information
Analysis ID
0ad962ec38dd14a782b15129df09c5ad
Registration Date
April 07, 2022
Manufacturer
Authorized Representative

