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

• 20889483221669 - Performance Home Medical: 2026-01-08 Composite Respiratory Kits, 2 - 16SOFT-4, 2 - 0556B, 1 - 0027B, 1 - 0052B, 1 - No Smoking Sign, 2 - 1220-0
• 10889483223314 - Pedi-Neb™: 2026-01-08 Pedi-Neb™ Nasal Nebulizer
• 30889483228108 - Cardinal Health: 2026-01-08 Anesthesia Breathing Circuit, 60" Pediatric Corrugated Tubing
• 30889483228115 - Cardinal Health: 2026-01-08 Anesthesia Breathing Circuit, 60" Pediatric Corrugated Tubing
• 30889483228122 - Cardinal Health: 2026-01-08 Anesthesia Breathing Circuit, 60" Pediatric Corrugated Tubing
• 30889483228139 - Cardinal Health: 2026-01-08 Anesthesia Breathing Circuit, 60" Pediatric Coaxial Tubing
• 30889483228146 - Cardinal Health: 2026-01-08 Anesthesia Breathing Circuit, 108" Pediatric Expandable Tubing
• 30889483228153 - Cardinal Health: 2026-01-08 Anesthesia Breathing Circuit, 120" Pediatric Expandable Tubing