Vertebroplasty needles T060413B

GUDID 03760177045774

TEKNIMED

Vertebral body cement cannula Vertebral body cement cannula Vertebral body cement cannula Vertebral body cement cannula Vertebral body cement cannula Vertebral body cement cannula Vertebral body cement cannula Vertebral body cement cannula Vertebral body cement cannula Vertebral body cement cannula Vertebral body cement cannula Vertebral body cement cannula Vertebral body cement cannula Vertebral body cement cannula Vertebral body cement cannula Vertebral body cement cannula Vertebral body cement cannula

• Primary Device ID: 03760177045774
• NIH Device Record Key: 3877da29-0d75-4358-a2a8-a50545604b37
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Vertebroplasty needles
• Version Model Number: 13G & Biopsy needle
• Catalog Number: T060413B
• Company DUNS: 764746723
• Company Name: TEKNIMED
• 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: true
• 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

Device Identifiers

Device Issuing Agency	Device ID
GS1	03760177045774 [Primary]

FDA Product Code

• MJG: Device, Percutaneous, Biopsy

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: 2023-09-14
• Device Publish Date: 2023-09-06

On-Brand Devices [Vertebroplasty needles]

• 03760177045774: 13G & Biopsy needle
• 03760177045767: 13G
• 03760177045750: 11G & Biopsy needle
• 03760177045743: 11G