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L, DreamWisp Nasal, Med Connector w/Hgr, AP - FDA Registration 8acd797ebba198ad1cec2a1b8a3ead35

Access comprehensive regulatory information for L, DreamWisp Nasal, Med Connector w/Hgr, AP in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID 8acd797ebba198ad1cec2a1b8a3ead35 and manufactured by Respironics Medical Products (Shenzhen) Co., Ltd, China. The device was registered on March 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
8acd797ebba198ad1cec2a1b8a3ead35
L, DreamWisp Nasal, Med Connector w/Hgr, AP
FDA ID: 8acd797ebba198ad1cec2a1b8a3ead35
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Device Classification
Brand Name
PHILIPS RESPIRONICS
Registration Information
Analysis ID
8acd797ebba198ad1cec2a1b8a3ead35
Registration Date
March 29, 2022