G.E.B. tubing

GUDID 50800000828018

A1 SURGICAL SUPPLIES, LLC

Suction/irrigation tubing, single-use

• Primary Device ID: 50800000828018
• NIH Device Record Key: 94c50a53-3e7a-4f95-bd41-a90fa118368f
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: G.E.B. tubing
• Version Model Number: A
• Company DUNS: 081334483
• Company Name: A1 SURGICAL SUPPLIES, 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: false
• RX Perscription: false
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	10800000828010 [Primary]
GS1	50800000828018 [Package]; Contains: 10800000828010; Package: [50 Units]; In Commercial Distribution

FDA Product Code

• BYY: Tube, Aspirating, Flexible, Connecting

Sterilization

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

[50800000828018]

Ethylene Oxide

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 3
• Public Version Date: 2019-10-07
• Device Publish Date: 2018-09-21

On-Brand Devices [G.E.B. tubing]

• 50860000082810: Suction tube
• 50800000828018: A
• 50860000082803: A