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Cannula Fixation Film with U-notch (Waterproof) - FDA Registration be484b70b2af52dba3b4304af6ab2c90

Access comprehensive regulatory information for Cannula Fixation Film with U-notch (Waterproof) in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID be484b70b2af52dba3b4304af6ab2c90 and manufactured by Well Lead Medical Co.,Ltd. The device was registered on June 15, 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
be484b70b2af52dba3b4304af6ab2c90
Cannula Fixation Film with U-notch (Waterproof)
FDA ID: be484b70b2af52dba3b4304af6ab2c90
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Device Classification
Brand Name
carePLUS Brand
Registration Information
Analysis ID
be484b70b2af52dba3b4304af6ab2c90
Registration Date
June 15, 2022
Authorized Representative