KAMVAC 530010500

GUDID 20603295171505

KAMVAC MINI SUCTION TUBE

DEPUY ORTHOPAEDICS, INC.

Disposable vacuum tubing

• Primary Device ID: 20603295171505
• NIH Device Record Key: 36eeaea0-f362-4ace-a64d-5cbca56da6e4
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: KAMVAC
• Version Model Number: 5300-10-500
• Catalog Number: 530010500
• Company DUNS: 080506581
• Company Name: DEPUY ORTHOPAEDICS, 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)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx

Device Identifiers

Device Issuing Agency	Device ID
GS1	10603295171508 [Primary]
GS1	20603295171505 [Package]; Contains: 10603295171508; Package: BOX [20 Units]; In Commercial Distribution

FDA Product Code

• JOL: CATHETER AND TIP, SUCTION

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 3
• Public Version Date: 2022-07-04
• Device Publish Date: 2016-06-30

On-Brand Devices [KAMVAC]

• 20603295171512: KAMVAC CURVED MINI SUCTION TUBE
• 20603295171505: KAMVAC MINI SUCTION TUBE
• 20603295171499: KAMVAC STANDARD SUCTION TUBE