Uni-Flo 220490

GUDID 20857595005422

Uni-Flo™ Fenestrated Catheter – 5 inch (127mm), 19 GA x 36 in (914mm)

SUMMIT MEDICAL PRODUCTS, INC.

Anaesthesia conduction catheter

• Primary Device ID: 20857595005422
• NIH Device Record Key: 1d3d324e-daab-46d6-9c38-539e24fe7d7f
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Uni-Flo
• Version Model Number: 220490
• Catalog Number: 220490
• Company DUNS: 831704841
• Company Name: SUMMIT MEDICAL PRODUCTS, INC.
• 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: true
• 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: (801) 352-1888
• Email: service@ambitpump.com

Device Dimensions

• Length: 127 Millimeter

Device Identifiers

Device Issuing Agency	Device ID
GS1	00857595005428 [Primary]
GS1	20857595005422 [Package]; Contains: 00857595005428; Package: [10 Units]; In Commercial Distribution

FDA Product Code

• FRN: Pump, Infusion

Sterilization

• Steralize Prior To Use: false
• Device Is Sterile: true

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 6
• Public Version Date: 2019-02-07
• Device Publish Date: 2016-09-09

On-Brand Devices [Uni-Flo]

• 20857595005439: Uni-Flo™ Fenestrated Catheter – 10 inch (254mm), 19 GA x 36 in (914mm)
• 20857595005422: Uni-Flo™ Fenestrated Catheter – 5 inch (127mm), 19 GA x 36 in (914mm)
• 20857595005415: Uni-Flo™ Fenestrated Catheter – 2.5 inch (63.5 mm), 19 GA x 36 in (914mm)