KYPHON ELEMENT™ Balloon Kyphoplasty System

GUDID 00643169582231

BONE ACCESS TOOLS T25R VALUE BONE ACCESS

MEDTRONIC SOFAMOR DANEK, INC.

Bone access cannula

• Primary Device ID: 00643169582231
• NIH Device Record Key: ef1fefd9-eda9-414b-ab1f-033a3d34a966
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: KYPHON ELEMENT™ Balloon Kyphoplasty System
• Version Model Number: T25R
• Company DUNS: 830350380
• Company Name: MEDTRONIC SOFAMOR DANEK, 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: true
• Device Combination Product: false
• Single Use: true
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: false
• 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)633-8766
• Email: Corporate.UDI@medtronic.com
• Phone: +1(800)633-8766
• Email: Corporate.UDI@medtronic.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	00643169582231 [Primary]

FDA Product Code

• LXH: ORTHOPEDIC MANUAL SURGICAL INSTRUMENT

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 2
• Public Version Date: 2018-03-29
• Device Publish Date: 2017-10-14

On-Brand Devices [KYPHON ELEMENT™ Balloon Kyphoplasty System]

• 00643169582231: BONE ACCESS TOOLS T25R VALUE BONE ACCESS
• 00643169582248: BONE FILLER DEVICE F25R 3 VALUE BFD
• 20643169842735: BONE FILLER 7480703T BFD SIZE 3
• 00643169582224: INFLATION SYRINGE A25R VALUE SYRINGE