BleedStop™

GUDID 00850817006159

Box of 3 BleedStop™ Nosebleed Foam Strips

Coag Medical, LLC

Plant polysaccharide haemostatic agent, bioabsorbable

• Primary Device ID: 00850817006159
• NIH Device Record Key: ea515fb3-0cba-4f00-af6a-62a870b7619c
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: BleedStop™
• Version Model Number: BSP03NBS
• Company DUNS: 079736884
• Company Name: Coag Medical, 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: false
• Expiration Date: true
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: false
• OTC Over-The-Counter: true

Device Identifiers

Device Issuing Agency	Device ID
GS1	00850817006159 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K140313

FDA Product Code

• LYA: Splint, Intranasal Septal

Sterilization

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

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2025-08-08
• Device Publish Date: 2025-07-31

On-Brand Devices [BleedStop™]

• 00850817006494: BleedStop™ Nosebleed Foam Strip Large
• 00850817006463: Box of 4 BleedStop™ Nosebleed Foam Strips
• 00850817006326: BleedStop™ 150g pouch
• 00850817006265: Box of 4 BleedStop™ 15g pouches
• 00850817006258: BleedStop™ 20g pouch
• 00850817006241: BleedStop™ 60g pouch
• 00850817006159: Box of 3 BleedStop™ Nosebleed Foam Strips
• 00850817006142: Box of 2 BleedStop™ 20g pouches
• 00850817006135: Box of 3 BleedStop™ 15g pouches
• 00850817006111: Box of 5 BleedStop™ 15g pouches
• 00850817006067: BleedStop™ Nosebleed Foam Strip
• 00850817006005: BleedStop™ 15g pouch