Nixall

GUDID 00851608007232

Nixall Wound & Skin, 8oz.

Seriously Clean, Ltd.

Antimicrobial wound irrigation solution

• Primary Device ID: 00851608007232
• NIH Device Record Key: 2b77cc51-cefd-488a-b3ca-aa923ccfff5e
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Nixall
• Version Model Number: 811M1L
• Company DUNS: 020333292
• Company Name: Seriously Clean, Ltd.
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: false
• MRI Safety Status: Labeling does not contain MRI Safety Information
• Human Cell/Tissue Product: false
• Device Kit: false
• Device Combination Product: false
• Single Use: false
• Lot Batch: false
• Serial Number: false
• Manufacturing Date: false
• 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: true

Device Identifiers

Device Issuing Agency	Device ID
GS1	00851608007232 [Primary]

FDA Product Code

• FRO: Dressing, Wound, Drug

Sterilization

• Steralize Prior To Use: false
• Device Is Sterile: false

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2023-03-17
• Device Publish Date: 2023-03-09

On-Brand Devices [Nixall]

• 00851608007232: Nixall Wound & Skin, 8oz.
• 00851608007225: Nixall Wound & Skin, 2oz.
• 00851608007218: Nixall First Aid, 8oz.
• 00851608007201: Nixall First Aid Solution, 2oz.