Compress Bandage 24"x72"

GUDID 00840117332492

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 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: 00840117332492
• NIH Device Record Key: 5367fb53-fbcf-4ad2-b819-f841b40525aa
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Compress Bandage 24"x72"
• Version Model Number: 3202UB-1
• Company DUNS: 008124539
• Company Name: DYNAREX CORPORATION
• 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: false
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: false
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	00840117332485 [Package]; Package: Mc [50 Units]; In Commercial Distribution
GS1	00840117332492 [Package]; Contains: 00840117334618; Package: Box [1 Units]; In Commercial Distribution
GS1	00840117334618 [Primary]

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: 2024-04-02
• Device Publish Date: 2024-03-25

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• 00840117333000 - XeroBurn Sterile Burn Dressing Blanket: 2024-04-02 30" x 35"
• 00840117333024 - XeroBurn Sterile Burn Dressing Blanket 60"x 70": 2024-04-02 60"x 70"
• 00840117333048 - XeroBurn Sterile Burn Dressing Blanket 70" x 95": 2024-04-02 70" x 95"