Securis SEC0100

GUDID 20801741075456

SECURIS STABILIZATION DEVICE

Bard Access Systems, Inc.

Wearable percutaneous catheter/tube holder

• Primary Device ID: 20801741075456
• NIH Device Record Key: 4ee2a75c-ddf0-4d00-adb7-49d137031aef
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Securis
• Version Model Number: SEC0100
• Catalog Number: SEC0100
• Company DUNS: 044611812
• Company Name: Bard Access Systems, 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: true
• RX Perscription: true
• OTC Over-The-Counter: false

Customer Support Contacts

• Phone: +1(800)545-0890
• Email: medical.services@crbard.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	00801741075452 [Primary]
GS1	10801741075459 [Package]; Contains: 00801741075452; Package: CA [50 Units]; In Commercial Distribution
GS1	20801741075456 [Package]; Contains: 10801741075459; Package: BX [16 Units]; In Commercial Distribution

FDA Product Code

• KMK: DEVICE, INTRAVASCULAR CATHETER SECUREMENT

Sterilization

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

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2019-10-25
• Device Publish Date: 2019-10-17

On-Brand Devices [Securis]

• 10801741075466: SECURIS STABILIZATION DEVICE w/DFU, 1000 units, SECNS01
• 20801741075456: SECURIS STABILIZATION DEVICE
• 10801741085731: DOT SECURIS STABN DEVICE SEPP W/ALCOHOL