DynaSafety Heavy Duty Woven Fabric Bandages, Sterile, 7/8" x 1 1/2"

GUDID 00810180840569

STERILE-EO

Dynarex Corporation

Adhesive bandage

• Primary Device ID: 00810180840569
• NIH Device Record Key: 3bb0d210-e5f4-4b02-af37-ea2a3e216608
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: DynaSafety Heavy Duty Woven Fabric Bandages, Sterile, 7/8" x 1 1/2"
• Version Model Number: 3768-50
• 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	00810180840569 [Unit of Use]
GS1	00840117331952 [Package]; Contains: 00840117331969; Package: Case [25 Units]; In Commercial Distribution
GS1	00840117331969 [Primary]

FDA Product Code

• KGX: Tape And Bandage, Adhesive

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: 2024-03-08

On-Brand Devices [DynaSafety Heavy Duty Woven Fabric Bandages, Sterile, 7/8" x 1 1/2"]

• 08401173319692: STERILE-EO
• 00810180840569: STERILE-EO