Abdominal Aortic & Junctional Tourniquet (Stabilized) - AAJT-S

GUDID 00860002227504

Abdominal Aortic & Junctional Tourniquet (Stabilized) - AAJT-S

Compression Works, Inc.

Emergency junctional haemorrhage compression set Emergency junctional haemorrhage compression set Emergency junctional haemorrhage compression set Emergency junctional haemorrhage compression set Emergency junctional haemorrhage compression set Emergency junctional haemorrhage compression set Emergency junctional haemorrhage compression set Emergency junctional haemorrhage compression set Emergency junctional haemorrhage compression set Emergency junctional haemorrhage compression set Emergency junctional haemorrhage compression set Emergency junctional haemorrhage compression set Emergency junctional haemorrhage compression set Emergency junctional haemorrhage compression set Emergency junctional haemorrhage compression set Emergency junctional haemorrhage compression set Emergency junctional haemorrhage compression set

• Primary Device ID: 00860002227504
• NIH Device Record Key: 65dc4877-c50b-425a-903f-01b2aae9e5b8
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Abdominal Aortic & Junctional Tourniquet (Stabilized) - AAJT-S
• Version Model Number: AAJT-S001
• Company DUNS: 112559979
• Company Name: Compression Works, Inc.
• 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: false
• 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	00860002227504 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K221661

FDA Product Code

• DXC: Clamp, Vascular

Sterilization

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

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2023-03-28
• Device Publish Date: 2023-03-20