PureKit Gun MV

GUDID 03701505800498

TEKNIMED

Orthopaedic cement preparation/delivery kit

• Primary Device ID: 03701505800498
• NIH Device Record Key: 70775e5a-582d-4ba5-a8cb-c4e4094c577a
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: PureKit Gun MV
• Version Model Number: T060426MV
• Company DUNS: 764746723
• Company Name: TEKNIMED
• 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: 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	03701505800498 [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: 2023-04-07
• Device Publish Date: 2023-03-30

On-Brand Devices [PureKit Gun MV]

• 03701505800498: T060426MV
• 03760177045361: T060425MV