DynaSafety Heavy Duty Woven Fabric Knuckle Bandages, 1 1/2" x 3"

GUDID 00810180840620

STERILE-EO

Dynarex Corporation

Adhesive bandage

• Primary Device ID: 00810180840620
• NIH Device Record Key: 799a50eb-7470-4022-b4ee-c3c1b3cbe0b3
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: DynaSafety Heavy Duty Woven Fabric Knuckle Bandages, 1 1/2" x 3"
• Version Model Number: 3765BULK
• Company DUNS: 008124539
• Company Name: Dynarex Corporation
• Device Count: 1500
• 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: true
• 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	00810180840620 [Unit of Use]
GS1	00840117331822 [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: 2024-10-30
• Device Publish Date: 2024-03-08

On-Brand Devices [DynaSafety Heavy Duty Woven Fabric Knuckle Bandages, 1 1/2" x 3"]

• 00840117331839: STERILE-EO
• 08401173318220: STERILE-EO
• 00810180840620: STERILE-EO