Xpect

GUDID 00850053907142

Naloxone Opioid Overdose Kit

Cintas Corporation No. 2

First aid kit, medicated

• Primary Device ID: 00850053907142
• NIH Device Record Key: 375cb134-4c6d-44cf-a2e2-947a7852428b
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Xpect
• Version Model Number: 620859
• Company DUNS: 118376317
• Company Name: Cintas Corporation No. 2
• 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: true
• Device Combination Product: false
• Single Use: true
• 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	00850053907142 [Primary]

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: 2024-06-28
• Device Publish Date: 2024-06-20

On-Brand Devices [Xpect]

• 10850047958997: Polymer Patient Exam Gloves Large
• 00850053907142: Naloxone Opioid Overdose Kit