SunMed LLC AF5040MB-PWT

GUDID 30889483565630

AirFlow Adult Resuscitator with B/V Filter, Bag Reservoir, Mask, Attached PEEP Valve and 14' Tubing

SUNMED, LLC

Pulmonary resuscitator, manual, single-use Pulmonary resuscitator, manual, single-use Pulmonary resuscitator, manual, single-use Pulmonary resuscitator, manual, single-use Pulmonary resuscitator, manual, single-use Pulmonary resuscitator, manual, single-use Pulmonary resuscitator, manual, single-use Pulmonary resuscitator, manual, single-use Pulmonary resuscitator, manual, single-use Pulmonary resuscitator, manual, single-use Pulmonary resuscitator, manual, single-use Pulmonary resuscitator, manual, single-use Pulmonary resuscitator, manual, single-use Pulmonary resuscitator, manual, single-use Pulmonary resuscitator, manual, single-use Pulmonary resuscitator, manual, single-use Pulmonary resuscitator, manual, single-use

• Primary Device ID: 30889483565630
• NIH Device Record Key: 7f320543-039f-4edf-8e20-cd88c36f1a52
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: SunMed LLC
• Version Model Number: AF5040MB-PWT
• Catalog Number: AF5040MB-PWT
• Company DUNS: 069009268
• Company Name: SUNMED, LLC
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: false
• MRI Safety Status: MR Conditional
• 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: true
• 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: 18004332797
• Email: info@myairlife.com
• Phone: 18004332797
• Email: info@myairlife.com
• Phone: 18004332797
• Email: info@myairlife.com
• Phone: 18004332797
• Email: info@myairlife.com
• Phone: 18004332797
• Email: info@myairlife.com
• Phone: 18004332797
• Email: info@myairlife.com
• Phone: 18004332797
• Email: info@myairlife.com
• Phone: 18004332797
• Email: info@myairlife.com
• Phone: 18004332797
• Email: info@myairlife.com
• Phone: 18004332797
• Email: info@myairlife.com
• Phone: 18004332797
• Email: info@myairlife.com
• Phone: 18004332797
• Email: info@myairlife.com
• Phone: 18004332797
• Email: info@myairlife.com
• Phone: 18004332797
• Email: info@myairlife.com
• Phone: 18004332797
• Email: info@myairlife.com
• Phone: 18004332797
• Email: info@myairlife.com
• Phone: 18004332797
• Email: info@myairlife.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	10889483565636 [Primary]
GS1	30889483565630 [Package]; Contains: 10889483565636; Package: Case [10 Units]; In Commercial Distribution

FDA Product Code

• BTM: Ventilator, Emergency, Manual (Resuscitator)

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: 2023-11-01
• Device Publish Date: 2023-10-24

On-Brand Devices [SunMed LLC]

• 30889483553613: Pediatric, Noon-intubated, 7ft Oral/Nasal with Oxygen Tubing
• 30889483565630: AirFlow Adult Resuscitator with B/V Filter, Bag Reservoir, Mask, Attached PEEP Valve and 14' Tub