Leica Microsystems-M530 OHX - FDA Registration 6cfacc3df372c000a4d8337e7be31928
Access comprehensive regulatory information for Leica Microsystems-M530 OHX in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID 6cfacc3df372c000a4d8337e7be31928 and manufactured by Leica Instruments (Singapore) Pte Ltd. 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
6cfacc3df372c000a4d8337e7be31928
Leica Microsystems-M530 OHX
FDA ID: 6cfacc3df372c000a4d8337e7be31928
Device Classification
Brand Name
Leica
Registration Information
Analysis ID
6cfacc3df372c000a4d8337e7be31928
Registration Date
July 05, 2022
Manufacturer
Authorized Representative

