WaterPAP™ WP-7800

GUDID 10889483228715

WaterPAP™ Pro

SUNMED, LLC

PEEP valve, single-use

• Primary Device ID: 10889483228715
• NIH Device Record Key: 3713a74a-7c70-4726-8271-ee0446aa7883
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: WaterPAP™
• Version Model Number: WP-7800
• Catalog Number: WP-7800
• Company DUNS: 069009268
• Company Name: SUNMED, LLC
• 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: false
• Manufacturing Date: true
• Expiration Date: false
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: true
• OTC Over-The-Counter: false

Customer Support Contacts

• Phone: 1-800-433-2797
• Email: info@sun-med.com
• Phone: 1-800-433-2797
• Email: info@sun-med.com
• Phone: 1-800-433-2797
• Email: info@sun-med.com
• Phone: 1-800-433-2797
• Email: info@sun-med.com
• Phone: 1-800-433-2797
• Email: info@sun-med.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	00709078013201 [Previous]
GS1	10889483228715 [Primary]
GS1	20889483228712 [Package]; Package: Box [10 Units]; In Commercial Distribution
GS1	30889483228719 [Package]; Package: Case [40 Units]; In Commercial Distribution

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K110713

FDA Product Code

• BYE: Attachment, Breathing, Positive End Expiratory Pressure

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: 2025-12-23
• Device Publish Date: 2025-12-15

On-Brand Devices [WaterPAP™]

• 10889483228715: WaterPAP™ Pro
• 10889483228708: WaterPAP™