Benolar

GUDID 00850073690277

First Aid Solution 2oz

JOSH & BENI CORP

Antimicrobial wound irrigation solution

• Primary Device ID: 00850073690277
• NIH Device Record Key: 40c90480-6d7a-4146-ad03-4f3f348e6513
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Benolar
• Version Model Number: 1
• Company DUNS: 135730242
• Company Name: JOSH & BENI CORP
• 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: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	00850073690277 [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: 2025-04-22
• Device Publish Date: 2025-04-14

On-Brand Devices [Benolar]

• 00850073690307: Wound & Skin 8oz
• 00850073690291: Wound & Skin Solution 2oz
• 00850073690284: First Aid Solution 8oz
• 00850073690277: First Aid Solution 2oz