Aero-Pro

GUDID 10841470103757

ENGINEERED MEDICAL SYSTEMS INC

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• Primary Device ID: 10841470103757
• NIH Device Record Key: 809cd961-1002-484e-b6e2-2e4690c2620c
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Aero-Pro
• Version Model Number: 301-418
• Company DUNS: 154502934
• Company Name: ENGINEERED MEDICAL SYSTEMS INC
• 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: true
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: false
• Expiration Date: true
• 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	00841470103750 [Primary]
GS1	10841470103757 [Package]; Contains: 00841470103750; Package: [50 Units]; In Commercial Distribution

FDA Product Code

• CAH: Filter, Bacterial, Breathing-Circuit

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: 2023-12-19
• Device Publish Date: 2023-12-11

On-Brand Devices [Aero-Pro]

• 00841470108021: 301-439
• 10841470107137: 301-431
• 10841470103757: 301-418
• 10841470103436: 301-412
• 10841470100985: 301-411