HiVac™ 7 Triple Mix

GUDID 25060238200237

Bone Cement Mixing and Delivery System

SUMMIT MEDICAL LIMITED

Orthopaedic cement preparation/delivery kit

• Primary Device ID: 25060238200237
• NIH Device Record Key: bb4377d5-f691-49b5-bd60-1bb6212ff00f
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: HiVac™ 7 Triple Mix
• Version Model Number: C703
• Company DUNS: 221751311
• Company Name: SUMMIT MEDICAL LIMITED
• 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

Customer Support Contacts

• Phone: +441451821311
• Email: info@summit-medical.co.uk
• Phone: +441451821311
• Email: info@summit-medical.co.uk
• Phone: +441451821311
• Email: info@summit-medical.co.uk
• Phone: +441451821311
• Email: info@summit-medical.co.uk

Device Identifiers

Device Issuing Agency	Device ID
GS1	15060238200230 [Primary]
GS1	25060238200237 [Package]; Contains: 15060238200230; Package: Carton [5 Units]; In Commercial Distribution
GS1	35060238200234 [Package]; Package: Carton [10 Units]; In Commercial Distribution

FDA Product Code

• KIH: Dispenser, Cement

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: 2022-12-15
• Device Publish Date: 2022-12-07

On-Brand Devices [HiVac™ 7 Triple Mix ]

• 25060238200237: Bone Cement Mixing and Delivery System
• 25060238201630: HiVac™ 7 Triple Mix