Bard® Levin Duodenal Tube 0005530

GUDID 00801741076688

Bard® Levin Duodenal Tube

C. R. Bard, Inc.

Gastric lavage kit

• Primary Device ID: 00801741076688
• NIH Device Record Key: 0e260266-4b4e-416e-a2fb-774c2684dace
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Bard® Levin Duodenal Tube
• Version Model Number: 0005530
• Catalog Number: 0005530
• 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: true
• 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: 16 French
• Catheter Gauge: 16 French
• Catheter Gauge: 16 French
• Catheter Gauge: 16 French

Device Identifiers

Device Issuing Agency	Device ID
GS1	00801741076688 [Primary]

FDA Product Code

• FRQ: TUBE, LEVINE

Sterilization

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

[00801741076688]

Ethylene Oxide

[00801741076688]

Ethylene Oxide

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 2
• Public Version Date: 2018-03-29
• Device Publish Date: 2016-07-23

On-Brand Devices [Bard® Levin Duodenal Tube]

• 00801741076701: Bard® Levin Duodenal Tube
• 00801741076695: Bard® Levin Duodenal Tube
• 00801741076688: Bard® Levin Duodenal Tube
• 00801741076671: Bard® Levin Duodenal Tube
• 00801741076664: Bard® Levin Duodenal Tube
• 00801741076657: Bard® Levin Duodenal Tube