Compress Bandage - 36"x36

GUDID 00840117332478

DYNAREX CORPORATION

Absorbent wound compression pad

• Primary Device ID: 00840117332478
• NIH Device Record Key: c3ab962e-bc40-4b8b-9843-26ad5767e8b3
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Compress Bandage - 36"x36
• Version Model Number: 3201UB-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	00840117332461 [Package]; Package: Mc [50 Units]; In Commercial Distribution
GS1	00840117332478 [Package]; Contains: 00840117334601; Package: Box [1 Units]; In Commercial Distribution
GS1	00840117334601 [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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