Sure-Point® Table Mount D06000

GUDID 00801741079030

Sure-Point® Table Mount

C. R. Bard, Inc.

General-purpose brachytherapy system applicator, manual

• Primary Device ID: 00801741079030
• NIH Device Record Key: a78ba597-81db-49cd-ad6b-d4e60822baaf
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Sure-Point® Table Mount
• Version Model Number: D06000
• Catalog Number: D06000
• Company DUNS: 016898496
• Company Name: C. R. Bard, Inc.
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: false
• MRI Safety Status: Labeling does not contain MRI Safety Information
• Human Cell/Tissue Product: false
• Device Kit: false
• Device Combination Product: false
• Single Use: false
• Lot Batch: false
• Serial Number: true
• Manufacturing Date: true
• Expiration Date: false
• 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)977-6733
• Email: medical.services@crbard.com
• Phone: +1(800)977-6733
• Email: medical.services@crbard.com
• Phone: +1(800)977-6733
• Email: medical.services@crbard.com
• Phone: +1(800)977-6733
• Email: medical.services@crbard.com
• Phone: +1(800)977-6733
• Email: medical.services@crbard.com
• Phone: +1(800)977-6733
• Email: medical.services@crbard.com
• Phone: +1(800)977-6733
• Email: medical.services@crbard.com
• Phone: +1(800)977-6733
• Email: medical.services@crbard.com
• Phone: +1(800)977-6733
• Email: medical.services@crbard.com
• Phone: +1(800)977-6733
• Email: medical.services@crbard.com
• Phone: +1(800)977-6733
• Email: medical.services@crbard.com
• Phone: +1(800)977-6733
• Email: medical.services@crbard.com
• Phone: +1(800)977-6733
• Email: medical.services@crbard.com
• Phone: +1(800)977-6733
• Email: medical.services@crbard.com
• Phone: +1(800)977-6733
• Email: medical.services@crbard.com
• Phone: +1(800)977-6733
• Email: medical.services@crbard.com
• Phone: +1(800)977-6733
• Email: medical.services@crbard.com
• Phone: +1(800)977-6733
• Email: medical.services@crbard.com
• Phone: +1(800)977-6733
• Email: medical.services@crbard.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	00801741079030 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K972152

FDA Product Code

• ITX: Transducer, ultrasonic, diagnostic

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 3
• Public Version Date: 2018-07-06
• Device Publish Date: 2016-09-19

Devices Manufactured by C. R. Bard, Inc.

• 10801741127653 - Bard® X-Force® Nephrostomy Balloon Dilation Catheter: 2025-08-05 Bard® X-Force® Nephrostomy Balloon Dilation Catheter
• 10801741127660 - Bard® X-Force® Nephrostomy Balloon Dilation Catheter: 2025-08-05 Bard® X-Force® Nephrostomy Balloon Dilation Catheter
• 10801741011655 - Bard® Silicone Uretero-Intestinal Anastomosis Urinary Diversion Stent: 2025-04-25 Bard® Silicone Uretero-Intestinal Anastomosis Urinary Diversion Stent with Hydro-Glide™ Guidewire
• 10801741171809 - Bardia: 2025-03-18 Bardia Silicone Elastomer Coated Foley Catheter
• 10801741171816 - Bardia: 2025-03-18 Bardia Silicone Elastomer Coated Foley Catheter
• 10801741226967 - PureWick: 2024-08-06 PureWick Flex Female External Catheter, Acute Care
• 10801741226981 - PureWick: 2024-08-06 PureWick Flex Female External Catheter, Home Care
• 10801741226462 - PureWick: 2024-06-10 PureWick Male External Catheter, Home Care