Ultima Drive Activator C-UA-5001

GUDID 00607567700901

Ultima Drive Activator

MAQUET CARDIOVASCULAR LLC

Sternum spreader

• Primary Device ID: 00607567700901
• NIH Device Record Key: bade98f2-f6db-42eb-9527-77e2b1c82a5c
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Ultima Drive Activator
• Version Model Number: C-UA-5001
• Catalog Number: C-UA-5001
• Company DUNS: 022348156
• Company Name: MAQUET CARDIOVASCULAR LLC
• 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: false
• 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: 888-880-2874
• Email: cssurgery@maquet.com
• Phone: 888-880-2874
• Email: cssurgery@maquet.com
• Phone: 888-880-2874
• Email: cssurgery@maquet.com
• Phone: 888-880-2874
• Email: cssurgery@maquet.com
• Phone: 888-880-2874
• Email: cssurgery@maquet.com
• Phone: 888-880-2874
• Email: cssurgery@maquet.com
• Phone: 888-880-2874
• Email: cssurgery@maquet.com
• Phone: 888-880-2874
• Email: cssurgery@maquet.com
• Phone: 888-880-2874
• Email: cssurgery@maquet.com
• Phone: 888-880-2874
• Email: cssurgery@maquet.com
• Phone: 888-880-2874
• Email: cssurgery@maquet.com
• Phone: 888-880-2874
• Email: cssurgery@maquet.com
• Phone: 888-880-2874
• Email: cssurgery@maquet.com
• Phone: 888-880-2874
• Email: cssurgery@maquet.com
• Phone: 888-880-2874
• Email: cssurgery@maquet.com
• Phone: 888-880-2874
• Email: cssurgery@maquet.com
• Phone: 888-880-2874
• Email: cssurgery@maquet.com
• Phone: 888-880-2874
• Email: cssurgery@maquet.com
• Phone: 888-880-2874
• Email: cssurgery@maquet.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	00607567700901 [Primary]

FDA Product Code

• DWS: Instruments, Surgical, Cardiovascular

Sterilization

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

[00607567700901]

Moist Heat or Steam Sterilization

[00607567700901]

Moist Heat or Steam Sterilization

[00607567700901]

Moist Heat or Steam Sterilization

[00607567700901]

Moist Heat or Steam Sterilization

[00607567700901]

Moist Heat or Steam Sterilization

[00607567700901]

Moist Heat or Steam Sterilization

[00607567700901]

Moist Heat or Steam Sterilization

[00607567700901]

Moist Heat or Steam Sterilization

[00607567700901]

Moist Heat or Steam Sterilization

[00607567700901]

Moist Heat or Steam Sterilization

[00607567700901]

Moist Heat or Steam Sterilization

[00607567700901]

Moist Heat or Steam Sterilization

[00607567700901]

Moist Heat or Steam Sterilization

[00607567700901]

Moist Heat or Steam Sterilization

[00607567700901]

Moist Heat or Steam Sterilization

[00607567700901]

Moist Heat or Steam Sterilization

[00607567700901]

Moist Heat or Steam Sterilization

[00607567700901]

Moist Heat or Steam Sterilization

[00607567700901]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 2
• Public Version Date: 2018-03-29
• Device Publish Date: 2016-09-24

Devices Manufactured by MAQUET CARDIOVASCULAR LLC

• 00607567700307 - HeartString III Proximal Seal: 2025-02-06 HeartString III Proximal Seal
• 00607567700468 - Vasoshield: 2025-02-06 Vasoshield Pressure Controlling Syringe
• 00607567700598 - Axius Coronary Shunt: 2025-02-06 Axius Coronary Shunt
• 00607567700604 - Axius Coronary Shunt: 2025-02-06 Axius Coronary Shunt
• 00607567700611 - Axius Coronary Shunt: 2025-02-06 Axius Coronary Shunt
• 00607567700628 - Axius Coronary Shunt: 2025-02-06 Axius Coronary Shunt
• 00607567700635 - Axius Coronary Shunt: 2025-02-06 Axius Coronary Shunt
• 00607567700642 - Axius Coronary Shunt: 2025-02-06 Axius Coronary Shunt