PRO-NOX™ WES-PROSMLKIT

GUDID 20889483231750

Pro-Nox Small Adult Disposable Kit Patient Circuit, 77" Magenta Tubing, Small Adult Mask

SUNMED, LLC

Anaesthesia breathing circuit, single-use

• Primary Device ID: 20889483231750
• NIH Device Record Key: c2565817-a4b5-4866-aec0-89b57a761cb6
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: PRO-NOX™
• Version Model Number: WES-PROSMLKIT
• Catalog Number: WES-PROSMLKIT
• 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: false
• Expiration Date: false
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: true
• 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
• 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
• 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	00709078006708 [Previous]
GS1	10889483231753 [Primary]
GS1	20889483231750 [Package]; Contains: 10889483231753; Package: Box [20 Units]; In Commercial Distribution

FDA Product Code

• CAH: Filter, Bacterial, Breathing-Circuit

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: 2026-01-07
• Device Publish Date: 2025-12-30

Devices Manufactured by SUNMED, LLC

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• 30889483562615 - BALLARD™: 2026-02-06 BALLARD™ TURBO-CLEANING CLOSED SUCTION SYSTEM FOR ADULTS, Double Swivel Elbow, Endotracheal
• 30889483563391 - BALLARD™: 2026-02-06 BALLARD™ ORAL CARE SUCTION CATHETER FOR ADULTS
• 30889483563681 - BALLARD™: 2026-02-06 BALLARD™ CLOSED SUCTION SYSTEM FOR NEONATES/PEDIATRICS, Y-Adapter, Endotracheal, WET PAK™
• 30889483563711 - BALLARD™: 2026-02-06 BALLARD™ CLOSED SUCTION SYSTEM FOR NEONATES/PEDIATRICS, Y-Adapter, Endotracheal, WET PAK™
• 30889483567030 - BALLARD™: 2026-02-06 BALLARD™ CLOSED SUCTION SYSTEM FOR NEONATES/PEDIATRICS, Elbow, Endotracheal, WET PAK™
• 30889483623316 - BALLARD™: 2026-02-06 BALLARD™ CLOSED SUCTION SYSTEM FOR ADULTS, Double Swivel Elbow, Tracheostomy, 12 F