Aero-T+

GUDID 10841470103740

ENGINEERED MEDICAL SYSTEMS INC

Heat/moisture exchanger, single-use

• Primary Device ID: 10841470103740
• NIH Device Record Key: 053eb2e0-1a3c-4f8f-bf26-0c253bf26e79
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Aero-T+
• Version Model Number: 301-401
• Company DUNS: 154502934
• Company Name: ENGINEERED MEDICAL SYSTEMS INC
• 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: 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	00841470103743 [Primary]
GS1	10841470103740 [Package]; Contains: 00841470103743; Package: [50 Units]; In Commercial Distribution

FDA Product Code

• BYD: Condenser, Heat And Moisture (Artificial Nose)

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

Devices Manufactured by ENGINEERED MEDICAL SYSTEMS INC

• 10841470106215 - ABC -Flex Tube System: 2025-04-21
• 10841470106260 - ABC - Uniflow Breathing Circuit: 2025-04-21
• 10841470106284 - ABC - Duoflow Bi-lumen Breathing Circuit: 2025-04-21
• 10841470106345 - ABC - Flex Tube System: 2025-04-21
• 10841470106574 - ABC - Compact Breathing Circuit: 2025-04-21
• 10841470106581 - ABC - Compact Breathing Circuit: 2025-04-21
• 10841470106734 - ABC - Duoflow Bi-lumen Breathing Circuit: 2025-04-21
• 10841470107113 - ABC - Uniflow Breathing Circuit: 2025-04-21