Coleman

GUDID 00368093000070

First Aid Kit

WISCONSIN PHARMACAL COMPANY, LLC

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• Primary Device ID: 00368093000070
• NIH Device Record Key: 9ce58f2e-0d99-4a59-9f37-53215a7a137b
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Coleman
• Version Model Number: 7605
• Company DUNS: 800873986
• Company Name: WISCONSIN PHARMACAL COMPANY, LLC
• 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: true
• 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	00368093000070 [Primary]

FDA Product Code

• LRR: First Aid Kit With 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: 2023-11-10
• Device Publish Date: 2023-11-02

On-Brand Devices [Coleman]

• 00368093000087: Coleman Waterproof First Aid Kit
• 00368093000070: First Aid Kit