SureStep Foley Tray System A309516AMS

GUDID 10801741218634

SureStep Foley Tray Kit optimized for Sensica UO System

C. R. Bard, Inc.

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• Primary Device ID: 10801741218634
• NIH Device Record Key: 12c12bdd-cb5f-41b6-bb32-a476dd298878
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: SureStep Foley Tray System
• Version Model Number: A309516AMS
• Catalog Number: A309516AMS
• Company DUNS: 016898496
• Company Name: C. R. Bard, Inc.
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: false
• MRI Safety Status: MR Conditional
• Human Cell/Tissue Product: false
• Device Kit: true
• Device Combination Product: true
• 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(844)823-5433
• Email: BMD.CS.support@bd.com
• Phone: +1(844)823-5433
• Email: BMD.CS.support@bd.com
• Phone: +1(844)823-5433
• Email: BMD.CS.support@bd.com
• Phone: +1(844)823-5433
• Email: BMD.CS.support@bd.com
• Phone: +1(844)823-5433
• Email: BMD.CS.support@bd.com
• Phone: +1(844)823-5433
• Email: BMD.CS.support@bd.com
• Phone: +1(844)823-5433
• Email: BMD.CS.support@bd.com
• Phone: +1(844)823-5433
• Email: BMD.CS.support@bd.com
• Phone: +1(844)823-5433
• Email: BMD.CS.support@bd.com
• Phone: +1(844)823-5433
• Email: BMD.CS.support@bd.com
• Phone: +1(844)823-5433
• Email: BMD.CS.support@bd.com
• Phone: +1(844)823-5433
• Email: BMD.CS.support@bd.com
• Phone: +1(844)823-5433
• Email: BMD.CS.support@bd.com
• Phone: +1(844)823-5433
• Email: BMD.CS.support@bd.com
• Phone: +1(844)823-5433
• Email: BMD.CS.support@bd.com
• Phone: +1(844)823-5433
• Email: BMD.CS.support@bd.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	00801741218637 [Primary]
GS1	10801741218634 [Package]; Contains: 00801741218637; Package: CA [10 Units]; In Commercial Distribution

FDA Product Code

• MJC: Catheter, urological (antimicrobial) and accessories

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: 2022-03-31
• Device Publish Date: 2022-03-23

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