DynaSafety Gauze Roll Bandages, Sterile, 3"

GUDID 00810180840262

Offset

Dynarex Corporation

Absorbent wound compression pad

• Primary Device ID: 00810180840262
• 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	00810180840262 [Unit of Use]
GS1	00840117332409 [Package]; Contains: 00840117332416; Package: Case [100 Units]; In Commercial Distribution
GS1	00840117332416 [Primary]

FDA Product Code

• FQM: Bandage, Elastic

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: 2024-10-29
• Device Publish Date: 2024-03-14

On-Brand Devices [DynaSafety Gauze Roll Bandages, Sterile, 3"]

• 08401173324160: Offset
• 00810180840262: Offset