Susol® Ribbon Tourniquet

GUDID 05060418837013

BAILEY INSTRUMENTS LTD

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• Primary Device ID: 05060418837013
• NIH Device Record Key: 396ff795-ff89-43ec-9f68-e09ee2c44f6f
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Susol® Ribbon Tourniquet
• Version Model Number: S-TQR-F
• Company DUNS: 769260357
• Company Name: BAILEY INSTRUMENTS LTD
• 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: true
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: true
• Expiration Date: true
• 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
GS1	05060418837013 [Package]; Contains: 05060418837020; Package: Pack [10 Units]; In Commercial Distribution
GS1	05060418837020 [Primary]

FDA Product Code

• GAX: Tourniquet, Nonpneumatic

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: 2024-01-31
• Device Publish Date: 2024-01-23

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