Fusion Vascular Grafts M002015010680

GUDID 00384409005614

Fusion 8mm-60cm Unsupp Peripheral Graft

MAQUET CARDIOVASCULAR LLC

Synthetic vascular graft Synthetic vascular graft Synthetic vascular graft Synthetic vascular graft Synthetic vascular graft Synthetic vascular graft Synthetic vascular graft Synthetic vascular graft Synthetic vascular graft Synthetic vascular graft Synthetic vascular graft Synthetic vascular graft Synthetic vascular graft

• Primary Device ID: 00384409005614
• NIH Device Record Key: b431944b-1aa3-4620-90b4-773207e3aae2
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Fusion Vascular Grafts
• Version Model Number: M002015010680
• Catalog Number: M002015010680
• Company DUNS: 022348156
• Company Name: MAQUET CARDIOVASCULAR LLC
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: false
• MRI Safety Status: MR Safe
• Human Cell/Tissue Product: false
• Device Kit: false
• Device Combination Product: false
• Single Use: true
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: false
• Expiration Date: true
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: true
• 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

Device Dimensions

• Lumen/Inner Diameter: 8 Millimeter
• Lumen/Inner Diameter: 8 Millimeter
• Length: 60 Centimeter
• Lumen/Inner Diameter: 8 Millimeter
• Length: 60 Centimeter
• Lumen/Inner Diameter: 8 Millimeter
• Length: 60 Centimeter
• Lumen/Inner Diameter: 8 Millimeter
• Length: 60 Centimeter
• Lumen/Inner Diameter: 8 Millimeter
• Length: 60 Centimeter
• Lumen/Inner Diameter: 8 Millimeter
• Length: 60 Centimeter
• Lumen/Inner Diameter: 8 Millimeter
• Length: 60 Centimeter
• Lumen/Inner Diameter: 8 Millimeter
• Length: 60 Centimeter
• Lumen/Inner Diameter: 8 Millimeter
• Length: 60 Centimeter
• Lumen/Inner Diameter: 8 Millimeter
• Length: 60 Centimeter
• Lumen/Inner Diameter: 8 Millimeter
• Length: 60 Centimeter
• Lumen/Inner Diameter: 8 Millimeter
• Length: 60 Centimeter
• Lumen/Inner Diameter: 8 Millimeter

Operating and Storage Conditions

• Special Storage Condition, Specify: Between 0 and 0 *Store at Controlled Room Temperature
• Special Storage Condition, Specify: Between 0 and 0 *Store at Controlled Room Temperature
• Special Storage Condition, Specify: Between 0 and 0 *Store at Controlled Room Temperature
• Special Storage Condition, Specify: Between 0 and 0 *Store at Controlled Room Temperature
• Special Storage Condition, Specify: Between 0 and 0 *Store at Controlled Room Temperature
• Special Storage Condition, Specify: Between 0 and 0 *Store at Controlled Room Temperature
• Special Storage Condition, Specify: Between 0 and 0 *Store at Controlled Room Temperature
• Special Storage Condition, Specify: Between 0 and 0 *Store at Controlled Room Temperature
• Special Storage Condition, Specify: Between 0 and 0 *Store at Controlled Room Temperature
• Special Storage Condition, Specify: Between 0 and 0 *Store at Controlled Room Temperature
• Special Storage Condition, Specify: Between 0 and 0 *Store at Controlled Room Temperature
• Special Storage Condition, Specify: Between 0 and 0 *Store at Controlled Room Temperature
• Special Storage Condition, Specify: Between 0 and 0 *Store at Controlled Room Temperature

Device Identifiers

Device Issuing Agency	Device ID
GS1	00384409005614 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K131778

FDA Product Code

• DSY: Prosthesis, Vascular Graft, Of 6mm And Greater Diameter

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 3
• Public Version Date: 2018-07-06
• Device Publish Date: 2015-10-24

On-Brand Devices [Fusion Vascular Grafts]

• 00384409005669: Fusion 8mm-80cm Unsupp Peripheral Graft
• 00384409005652: Fusion 7mm-80cm unsupp peripheral graft
• 00384409005645: Fusion 6mm-80cm Unsupp Peripheral Graft
• 00384409005638: Fusion 5mm-80cm unsupp peripheral graft
• 00384409005621: Fusion 10mm-80cm unsupp peripheral graft
• 00384409005614: Fusion 8mm-60cm Unsupp Peripheral Graft
• 00384409005607: Fusion 6mm-60cm Unsupp Peripheral Graft
• 00384409005591: Fusion 8mm-40cm Unsupp Peripheral Graft
• 00384409005584: Fusion 7mm-40cm unsupp peripheral graft
• 00384409005577: Fusion 6mm-40cm Unsupp Peripheral Graft
• 00384409005560: Fusion 5mm-40cm unsupp peripheral graft
• 00384409005553: Fusion 10mm-40cm unsupp peripheral graft
• 00384409005546: Fusion 6mm-20cm Unsupp Peripheral Graft