SunMed LLC 5807F-SE

GUDID 30889483553613

Pediatric, Noon-intubated, 7ft Oral/Nasal with Oxygen Tubing

SUNMED, LLC

Oxygen administration tubing

• Primary Device ID: 30889483553613
• NIH Device Record Key: 23a15f31-fac2-4ac3-90e4-28c51bbdbe88
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: SunMed LLC
• Version Model Number: 5807F-SE
• Catalog Number: 5807F-SE
• Company DUNS: 069009268
• Company Name: SUNMED, LLC
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: true
• 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: 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 Dimensions

• Length: 7 Feet
• Length: 7 Feet
• Length: 7 Feet
• Length: 7 Feet
• Length: 7 Feet
• Length: 7 Feet
• Length: 7 Feet
• Length: 7 Feet
• Length: 7 Feet
• Length: 7 Feet
• Length: 7 Feet
• Length: 7 Feet
• Length: 7 Feet
• Length: 7 Feet
• Length: 7 Feet
• Length: 7 Feet

Device Identifiers

Device Issuing Agency	Device ID
GS1	10889483553619 [Primary]
GS1	30889483553613 [Package]; Contains: 10889483553619; Package: CS [25 Units]; In Commercial Distribution

FDA Product Code

• BYX: Tubing, Pressure And Accessories

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: 2023-04-27
• Device Publish Date: 2023-04-19

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
• 20889483047917: IGuard Pediatric Eye Protector E-Series/Non-Sterile