Aortic Cutter 4.3MM AC-3043

GUDID 00607567700271

Aortic Cutter 4.3MM

MAQUET CARDIOVASCULAR LLC

Aorta punch, single-use

• Primary Device ID: 00607567700271
• NIH Device Record Key: 593d03b4-3675-4b9a-9033-198a5d84b5a6
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Aortic Cutter 4.3MM
• Version Model Number: AC-3043
• Catalog Number: AC-3043
• 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: 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: 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

Device Dimensions

• Outer Diameter: 4.3 Millimeter
• Outer Diameter: 4.3 Millimeter
• Outer Diameter: 4.3 Millimeter

Device Identifiers

Device Issuing Agency	Device ID
GS1	00607567700271 [Package]; Contains: 00607567700277; Package: 5 pack box [5 Units]; Discontinued: 2018-05-29; Not in Commercial Distribution
GS1	00607567700277 [Primary]
GS1	20607567700271 [Package]; Contains: 00607567700277; Package: 5 pack box [5 Units]; In Commercial Distribution

FDA Product Code

• FZT: Cutter, Surgical

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: 2018-05-30
• Device Publish Date: 2016-09-24

On-Brand Devices [Aortic Cutter 4.3MM]

• 00607567700271: Aortic Cutter 4.3MM
• 00607567700277: Aortic Cutter 4.3MM