DynaSafety Trauma2 Tourniquets

GUDID 08401173364692

Non-Sterile

DYNAREX CORPORATION

Arterial tourniquet, manual, single-use

• Primary Device ID: 08401173364692
• NIH Device Record Key: 72a6e725-154f-4820-bb33-9b304c5f69a9
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: DynaSafety Trauma2 Tourniquets
• Version Model Number: 3135
• Company DUNS: 008124539
• Company Name: DYNAREX CORPORATION
• Device Count: 50
• 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: false
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: true
• RX Perscription: false
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	00840117336469 [Primary]
GS1	08401173364692 [Unit of Use]

FDA Product Code

• GAX: Tourniquet, Nonpneumatic

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: 2024-06-25
• Device Publish Date: 2024-06-17

On-Brand Devices [DynaSafety Trauma2 Tourniquets ]

• 08401173364692: Non-Sterile
• 00810180840118: Non-Sterile