MicroSurge SUT-M110

GUDID 10817278011952

Mini Suture Guide

Alliant Enterprises, LLC

Operative-site suture holder Operative-site suture holder Operative-site suture holder Operative-site suture holder Operative-site suture holder Operative-site suture holder Operative-site suture holder Operative-site suture holder Operative-site suture holder Operative-site suture holder Operative-site suture holder Operative-site suture holder Operative-site suture holder Operative-site suture holder Operative-site suture holder Operative-site suture holder Operative-site suture holder Operative-site suture holder Operative-site suture holder Operative-site suture holder Operative-site suture holder Operative-site suture holder Operative-site suture holder Operative-site suture holder Operative-site suture holder Operative-site suture holder Operative-site suture holder Operative-site suture holder Operative-site suture holder Operative-site suture holder Operative-site suture holder Operative-site suture holder

• Primary Device ID: 10817278011952
• NIH Device Record Key: d8cee7a8-6503-4263-ab53-8c06eb5070dc
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: MicroSurge
• Version Model Number: SUT-M110
• Catalog Number: SUT-M110
• Company DUNS: 121170653
• Company Name: Alliant Enterprises, 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: 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	00817278011955 [Primary]
GS1	10817278011952 [Package]; Contains: 00817278011955; Package: Case [25 Units]; In Commercial Distribution

FDA Product Code

• GEJ: Carrier, Ligature

Sterilization

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

[10817278011952]

Ethylene Oxide

[10817278011952]

Ethylene Oxide

[10817278011952]

Ethylene Oxide

[10817278011952]

Ethylene Oxide

[10817278011952]

Ethylene Oxide

[10817278011952]

Ethylene Oxide

[10817278011952]

Ethylene Oxide

[10817278011952]

Ethylene Oxide

[10817278011952]

Ethylene Oxide

[10817278011952]

Ethylene Oxide

[10817278011952]

Ethylene Oxide

[10817278011952]

Ethylene Oxide

[10817278011952]

Ethylene Oxide

[10817278011952]

Ethylene Oxide

[10817278011952]

Ethylene Oxide

[10817278011952]

Ethylene Oxide

[10817278011952]

Ethylene Oxide

[10817278011952]

Ethylene Oxide

[10817278011952]

Ethylene Oxide

[10817278011952]

Ethylene Oxide

[10817278011952]

Ethylene Oxide

[10817278011952]

Ethylene Oxide

[10817278011952]

Ethylene Oxide

[10817278011952]

Ethylene Oxide

[10817278011952]

Ethylene Oxide

[10817278011952]

Ethylene Oxide

[10817278011952]

Ethylene Oxide

[10817278011952]

Ethylene Oxide

[10817278011952]

Ethylene Oxide

[10817278011952]

Ethylene Oxide

[10817278011952]

Ethylene Oxide

[10817278011952]

Ethylene Oxide

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 3
• Public Version Date: 2020-06-23
• 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