DynaSafety Gauze Roll Bandages, Sterile, 3"

GUDID 08401173324160

Offset

DYNAREX CORPORATION

Absorbent wound compression pad Absorbent wound compression pad Absorbent wound compression pad Absorbent wound compression pad Absorbent wound compression pad Absorbent wound compression pad Absorbent wound compression pad Absorbent wound compression pad Absorbent wound compression pad Absorbent wound compression pad Absorbent wound compression pad Absorbent wound compression pad Absorbent wound compression pad Absorbent wound compression pad Absorbent wound compression pad Absorbent wound compression pad

• Primary Device ID: 08401173324160
• NIH Device Record Key: 250754ca-0bb3-45e9-a2f8-fe83666431a2
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: DynaSafety Gauze Roll Bandages, Sterile, 3"
• Version Model Number: 3193UB-2
• Company DUNS: 008124539
• Company Name: DYNAREX CORPORATION
• Device Count: 2
• 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: true
• RX Perscription: false
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	00840117332409 [Package]; Contains: 00840117332416; Package: Case [100 Units]; In Commercial Distribution
GS1	00840117332416 [Primary]
GS1	08401173324160 [Unit of Use]

FDA Product Code

• FQM: Bandage, Elastic

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: 2024-03-22
• Device Publish Date: 2024-03-14

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