IntelliGuard® Anesthesia

GUDID 00860011670902

IntelliGuard Group, LLC

Anaesthesia cabinet

• Primary Device ID: 00860011670902
• NIH Device Record Key: 4b9435dc-170b-4589-a409-67b3fe9d4f56
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: IntelliGuard® Anesthesia
• Version Model Number: 5700-AS
• Company DUNS: 963409581
• Company Name: IntelliGuard Group, 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: 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: true
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	00860011670902 [Primary]

FDA Product Code

• BRY: Cabinet, Table And Tray, Anesthesia

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: 2024-04-09
• Device Publish Date: 2024-04-01