Propper Velket Tourniquet 22101100

GUDID 10818087011652

Velket - Single, Adult Size, Universal

PROPPER MANUFACTURING COMPANY, INC.

Arm/leg tourniquet, reusable Arm/leg tourniquet, reusable Arm/leg tourniquet, reusable Arm/leg tourniquet, reusable Arm/leg tourniquet, reusable Arm/leg tourniquet, reusable Arm/leg tourniquet, reusable Arm/leg tourniquet, reusable Arm/leg tourniquet, reusable Arm/leg tourniquet, reusable Limb tourniquet, manual, reusable Limb tourniquet, manual, reusable Limb tourniquet, manual, reusable Limb tourniquet, manual, reusable Limb tourniquet, manual, reusable Limb tourniquet, manual, reusable

• Primary Device ID: 10818087011652
• NIH Device Record Key: 1b4c3041-aea8-424e-8003-393d6dddf47f
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Propper Velket Tourniquet
• Version Model Number: 22101100
• Catalog Number: 22101100
• Company DUNS: 001483130
• Company Name: PROPPER MANUFACTURING COMPANY, INC.
• Device Count: 1
• 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: false
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: false
• Expiration Date: true
• Donation Id Number: false
• Contains Natural Rubber Latex: true
• Labeled No Natural Rubber Latex: false
• RX Perscription: false
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	10818087011652 [Primary]

FDA Product Code

• GAX: Tourniquet, Nonpneumatic

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 3
• Public Version Date: 2020-10-06
• Device Publish Date: 2017-10-16

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