Leica Microsystems-PROVEO 8 - FDA Registration a5b73513aecc2175cb2052d0775bd26c
Access comprehensive regulatory information for Leica Microsystems-PROVEO 8 in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID a5b73513aecc2175cb2052d0775bd26c and manufactured by Leica Instruments (Singapore) Pte Ltd. The device was registered on March 11, 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
a5b73513aecc2175cb2052d0775bd26c
Leica Microsystems-PROVEO 8
FDA ID: a5b73513aecc2175cb2052d0775bd26c
Device Classification
Brand Name
Leica
Registration Information
Analysis ID
a5b73513aecc2175cb2052d0775bd26c
Registration Date
March 11, 2022
Manufacturer
Authorized Representative

