Dynamo 11-5921

GUDID 03701505801211

TEKNIMED

Orthopaedic cement preparation/delivery kit

• Primary Device ID: 03701505801211
• NIH Device Record Key: 89985ec7-349b-49f8-a79a-623eeec04536
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Dynamo
• Version Model Number: Spinal Cement System Syringe MV 1.5cc
• Catalog Number: 11-5921
• 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: true
• 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	03701505801211 [Primary]

FDA Product Code

• NDN: Cement, Bone, Vertebroplasty

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: 2026-02-10
• Device Publish Date: 2026-02-02

On-Brand Devices [Dynamo]

• 03701505801235: Spinal Cement System Gun MV
• 03701505801228: Spinal Cement System Syringe MV 4cc
• 03701505801211: Spinal Cement System Syringe MV 1.5cc
• 03701505801204: Spinal Cement – MV