CrOC 31-200

GUDID M68931200060

The CRoC is indicated for use in the battlefield to control difficult bleeds in the inguinal and axilla areas. The CRoC is also indicated for use in the battlefield as a last resort for life threatening bleeds of the carotid artery. The CRoC should be applied by a trained medical provider.

Safeguard US Operating, LLC

Emergency junctional haemorrhage compression set

• Primary Device ID: M68931200060
• NIH Device Record Key: 154523a9-f266-40af-8bca-e28aa78e54af
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: CrOC
• Version Model Number: 06
• Catalog Number: 31-200
• Company DUNS: 118492643
• Company Name: Safeguard US Operating, 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: 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
HIBCC	M68931200060 [Primary]

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: 2024-11-08
• Device Publish Date: 2024-10-31

On-Brand Devices [CrOC]

• M68931200C0: The CRoC is indicated for use in the battlefield to control difficult bleeds in the inguinal and
• M68931200060: The CRoC is indicated for use in the battlefield to control difficult bleeds in the inguinal and