MVAP Comfort Sleep Nasal Cannula

GUDID 20889483225292

MVAP Comfort Sleep Nasal Cannula

SALTER LABS

Respiratory apnoea monitoring system

• Primary Device ID: 20889483225292
• NIH Device Record Key: 0e2e4951-5aee-4d97-8417-09bb37d83292
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: MVAP Comfort Sleep Nasal Cannula
• Version Model Number: SDC84
• Company DUNS: 022721133
• Company Name: SALTER LABS
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: false
• MRI Safety Status: Labeling does not contain MRI Safety Information
• Human Cell/Tissue Product: false
• Device Kit: false
• Device Combination Product: false
• Single Use: true
• Lot Batch: true
• Serial Number: true
• Manufacturing Date: true
• Expiration Date: true
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: true
• RX Perscription: true
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	10889483225295 [Primary]
GS1	20889483225292 [Package]; Contains: 10889483225295; Package: [50 Units]; In Commercial Distribution

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K151874

FDA Product Code

• BZQ: Monitor, Breathing Frequency

Sterilization

• Steralize Prior To Use: false
• Device Is Sterile: false

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2026-03-23
• Device Publish Date: 2026-03-13

On-Brand Devices [MVAP Comfort Sleep Nasal Cannula]

• 20889483225292: MVAP Comfort Sleep Nasal Cannula
• 20889483224363: MVAP Comfort Sleep Nasal Cannula