BloodSTOP iX Trauma Matrix

GUDID 00850744001449

BloodSTOP iX Trauma Matrix Hemostat pre hospital 3.5"X21" ( 8.75cmX52.5cm) z-folded 6 layers single pouch

Lifescience Plus, Inc.

Plant polysaccharide haemostatic agent, non-bioabsorbable, non-antimicrobial

• Primary Device ID: 00850744001449
• NIH Device Record Key: 724357da-bea2-4a8d-a6b1-975be9bafab6
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: BloodSTOP iX Trauma Matrix
• Version Model Number: TM-iX-26
• Company DUNS: 190600051
• Company Name: Lifescience Plus, 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: 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: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	00850744001449 [Primary]

FDA Product Code

• QSY: Hemostatic Wound Dressing Without Thrombin Or Other Biologics

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: 2024-07-03
• Device Publish Date: 2024-06-25

On-Brand Devices [BloodSTOP iX Trauma Matrix]

• 00850744001586: BloodSTOP IX Hemostat Trauma Care Matrix 12"X12" (30cmX30cm)
• 00850744001395: BloodSTOP IX Trauma Matrix 3"X24" (7.5cmX60cm) z-folded 8 layers
• 00850744001449: BloodSTOP iX Trauma Matrix Hemostat pre hospital 3.5"X21" ( 8.75cmX52.5cm) z-folded 6 layers si