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ROOM - FDA Registration 269abc64c75aa45b9f1eafe9b767ed9e

Access comprehensive regulatory information for ROOM in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID 269abc64c75aa45b9f1eafe9b767ed9e and manufactured by Roche Diagnostics GmbH. The device was registered on November 29, 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
269abc64c75aa45b9f1eafe9b767ed9e
ROOM
FDA ID: 269abc64c75aa45b9f1eafe9b767ed9e
Local name: SALI
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Device Classification
Brand Name
ROCHE
Registration Information
Analysis ID
269abc64c75aa45b9f1eafe9b767ed9e
Registration Date
November 29, 2022
Manufacturer
Authorized Representative