MicroSurge ANT-4012S

GUDID 00817278011788

Antegrade Cardioplegia Cannula w/Vent Line (12Ga) and insertion needle (14 ga), Low Profile, Ext Length

Alliant Enterprises, LLC

Cardioplegia cannula Cardioplegia cannula Cardioplegia cannula Cardioplegia cannula Cardioplegia cannula Cardioplegia cannula Cardioplegia cannula Cardioplegia cannula Cardioplegia cannula Cardioplegia cannula Cardioplegia cannula Cardioplegia cannula Cardioplegia cannula Cardioplegia cannula Cardioplegia cannula Cardioplegia cannula Cardioplegia cannula Cardioplegia cannula Cardioplegia cannula Cardioplegia cannula Cardioplegia cannula Cardioplegia cannula Cardioplegia cannula Cardioplegia cannula Cardioplegia cannula Cardioplegia cannula Cardioplegia cannula Cardioplegia cannula Cardioplegia cannula Cardioplegia cannula Cardioplegia cannula

• Primary Device ID: 00817278011788
• NIH Device Record Key: e007e45d-0f46-441e-8a60-7e4c69ef9573
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: MicroSurge
• Version Model Number: ANT-4012S
• Catalog Number: ANT-4012S
• Company DUNS: 121170653
• Company Name: Alliant Enterprises, LLC
• 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: 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

Device Identifiers

Device Issuing Agency	Device ID
GS1	00817278011788 [Package]; Package: Case [10 Units]; In Commercial Distribution
GS1	10817278011785 [Package]; Package: Case [10 Units]; In Commercial Distribution

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K964198

FDA Product Code

• DWF: Catheter, Cannula And Tubing, Vascular, Cardiopulmonary Bypass

Sterilization

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

[00817278011788]

Ethylene Oxide

[00817278011788]

Ethylene Oxide

[00817278011788]

Ethylene Oxide

[00817278011788]

Ethylene Oxide

[00817278011788]

Ethylene Oxide

[00817278011788]

Ethylene Oxide

[00817278011788]

Ethylene Oxide

[00817278011788]

Ethylene Oxide

[00817278011788]

Ethylene Oxide

[00817278011788]

Ethylene Oxide

[00817278011788]

Ethylene Oxide

[00817278011788]

Ethylene Oxide

[00817278011788]

Ethylene Oxide

[00817278011788]

Ethylene Oxide

[00817278011788]

Ethylene Oxide

[00817278011788]

Ethylene Oxide

[00817278011788]

Ethylene Oxide

[00817278011788]

Ethylene Oxide

[00817278011788]

Ethylene Oxide

[00817278011788]

Ethylene Oxide

[00817278011788]

Ethylene Oxide

[00817278011788]

Ethylene Oxide

[00817278011788]

Ethylene Oxide

[00817278011788]

Ethylene Oxide

[00817278011788]

Ethylene Oxide

[00817278011788]

Ethylene Oxide

[00817278011788]

Ethylene Oxide

[00817278011788]

Ethylene Oxide

[00817278011788]

Ethylene Oxide

[00817278011788]

Ethylene Oxide

[00817278011788]

Ethylene Oxide

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 3
• Public Version Date: 2018-07-06
• Device Publish Date: 2016-09-23

On-Brand Devices [MicroSurge]

• 10817278012317: Antegrade Cardioplegia Cannula (12ga) and Insertion Needle (14ga) Low Profile, Extended Length
• 10817278011990: BlowMister
• 10817278011969: Mini Suture Guide, 4 pack
• 10817278011952: Mini Suture Guide
• 00817278011788: Antegrade Cardioplegia Cannula w/Vent Line (12Ga) and insertion needle (14 ga), Low Profile, Ext
• 10817278011778: Antegrade Cardioplegia Cannula w/Vent Line (14Ga) and Insertion Needle (16ga), Low Profile, Exte
• 10817278011761: Antegrade Cardioplegia Cannula (14ga) and Insertion Needle (16ga) Low Profile, Extended Length