DynaSafety Sterile Gauze Pad, All Gauze

GUDID 00840117335868

3" x 3", 12-ply

DYNAREX CORPORATION

Woven gauze pad Woven gauze pad Woven gauze pad Woven gauze pad Woven gauze pad Woven gauze pad Woven gauze pad Woven gauze pad Woven gauze pad Woven gauze pad Woven gauze pad Woven gauze pad Woven gauze pad Woven gauze pad Woven gauze pad Woven gauze pad Woven gauze pad

• Primary Device ID: 00840117335868
• NIH Device Record Key: aca1b27d-ca15-4f47-95be-59bfa819c051
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: DynaSafety Sterile Gauze Pad, All Gauze
• Version Model Number: 3353UB-4
• 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: 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	00840117332560 [Package]; Contains: 00840117332577; Package: Case [100 Units]; In Commercial Distribution
GS1	00840117332577 [Package]; Package: Box [4 Units]; In Commercial Distribution
GS1	00840117335868 [Primary]

FDA Product Code

• NAB: Gauze / Sponge,Nonresorbable For External Use

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: 2024-03-26
• Device Publish Date: 2024-03-18

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