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Blood Collection Set (IMPROSAFE) - FDA Registration 2de0cccd435917387542d194e4390756

Access comprehensive regulatory information for Blood Collection Set (IMPROSAFE) in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID 2de0cccd435917387542d194e4390756 and manufactured by Guangzhou Improve Medical Instruments Co., Ltd. The device was registered on August 17, 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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2de0cccd435917387542d194e4390756
Blood Collection Set (IMPROSAFE)
FDA ID: 2de0cccd435917387542d194e4390756
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Device Classification
Brand Name
IMPROSAFE
Registration Information
Analysis ID
2de0cccd435917387542d194e4390756
Registration Date
August 17, 2022