Myanmar FDA registration 8acd797ebba198ad1cec2a1b8a3ead35
L, DreamWisp Nasal, Med Connector w/Hgr, AP
Device classification
- Brand Name
- PHILIPS RESPIRONICS
Registration information
- Analysis ID
- 8acd797ebba198ad1cec2a1b8a3ead35
- Registration Date
- March 29, 2022
Manufacturer
Authorized Representative
About this record
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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