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Sleep Screener - FDA Registration 6c2ca972aa28b59d9005cb97df41b4a6

Access comprehensive regulatory information for Sleep Screener in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID 6c2ca972aa28b59d9005cb97df41b4a6 and manufactured by Shenzhen Creative Industry Co., Ltd.. The device was registered on July 14, 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
6c2ca972aa28b59d9005cb97df41b4a6
Sleep Screener
FDA ID: 6c2ca972aa28b59d9005cb97df41b4a6
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Device Classification
Brand Name
Creative Medical
Registration Information
Analysis ID
6c2ca972aa28b59d9005cb97df41b4a6
Registration Date
July 14, 2022
Authorized Representative