Bard® Levin Tube 0044120

GUDID 20801741045770

Bard® Levin Tube

C. R. Bard, Inc.

Gastric lavage kit

• Primary Device ID: 20801741045770
• NIH Device Record Key: 721bddb0-7180-4e58-9d3b-431e27c5d297
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Bard® Levin Tube
• Version Model Number: 0044120
• Catalog Number: 0044120
• Company DUNS: 016898496
• Company Name: C. R. Bard, Inc.
• 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: 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: +1(800)526-4455
• Email: medical.services@crbard.com
• Phone: +1(800)526-4455
• Email: medical.services@crbard.com

Device Dimensions

• Catheter Gauge: 12 French
• Catheter Gauge: 12 French
• Catheter Gauge: 12 French
• Catheter Gauge: 12 French

Device Identifiers

Device Issuing Agency	Device ID
GS1	00801741045776 [Primary]
GS1	10801741045773 [Package]; Contains: 00801741045776; Package: BX [50 Units]; In Commercial Distribution
GS1	20801741045770 [Package]; Contains: 10801741045773; Package: CA [4 Units]; In Commercial Distribution

FDA Product Code

• FRQ: TUBE, LEVINE

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 2
• Public Version Date: 2018-03-29
• Device Publish Date: 2016-08-16

On-Brand Devices [Bard® Levin Tube]

• 20801741045800: Bard® Levin Tube
• 20801741045794: Bard® Levin Tube
• 10801741045780: Bard® Levin Tube
• 20801741045770: Bard® Levin Tube