RAPIDSTOP RSK501E

GUDID 09341394019409

First Aid Kit

AERO HEALTHCARE (US), LLC

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• Primary Device ID: 09341394019409
• NIH Device Record Key: a6ccdc58-e65e-4f9b-8f9d-45d2d0cdefcc
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: RAPIDSTOP
• Version Model Number: RSK501E
• Catalog Number: RSK501E
• Company DUNS: 008186174
• Company Name: AERO HEALTHCARE (US), 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: true
• 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	09341394019409 [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: 2023-12-18
• Device Publish Date: 2023-12-08

On-Brand Devices [RAPIDSTOP]

• 09341394033221: First Aid Kit
• 09341394033214: First Aid Kit
• 09341394033207: First Aid Kit
• 09341394019423: First Aid Kit
• 09341394019416: First Aid Kit
• 09341394019409: First Aid Kit
• 09341394019393: First Aid Kit
• 09341394019386: First Aid Kit
• 09341394019379: First Aid Kit