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Sign in to claim this brandAirlife, Inc.
US
Last updated May 23, 2026
What Airlife, Inc. makes
Airlife, Inc. manufactures single-use anaesthesia and ventilator breathing circuits, manual pulmonary resuscitators, reusable electrocardiographic lead sets, and single-use connectors for respiratory support. Their portfolio also includes benchtop therapeutic agent nebulizers, single-use cardiopulmonary resuscitation kits, and single-use electrocardiographic electrodes.
These devices are classified under FDA’s Class I and Class II categories and are listed in the FDA’s UDI (Unique Device Identification) database. The company is based in the United States.
Written from this company's registered devices by an AI model, and not verified by a human reviewer.
Frequently asked questions
What types of medical devices does Airlife, Inc. manufacture?
Airlife, Inc. specializes in respiratory and cardiac support devices. Their product portfolio includes single-use anaesthesia and ventilator breathing circuits, manual pulmonary resuscitators, reusable electrocardiographic lead sets, and single-use connectors for respiratory systems. They also produce benchtop therapeutic agent nebulizers, single-use cardiopulmonary resuscitation kits, and single-use electrocardiographic electrodes. These devices are designed for critical care, anaesthesia, and emergency resuscitation settings.
Where is Airlife, Inc. based?
Airlife, Inc. is headquartered in the United States. The company’s location in the US aligns with regulatory frameworks like the FDA’s UDI database, where their devices are listed for traceability and compliance purposes.
Which regulatory registries list Airlife, Inc.’s devices?
Airlife, Inc.’s devices are listed in the FDA’s Unique Device Identification (UDI) database. This registry ensures transparency and traceability of medical devices under FDA oversight, particularly for Class I and Class II products, which require identification for regulatory tracking.
How are Airlife, Inc.’s devices classified under FDA regulations?
Airlife, Inc.’s devices fall into FDA’s Class I and Class II categories. Class I devices generally pose minimal risk and often require general controls, while Class II devices involve a higher level of risk and may require special controls to ensure safety and effectiveness. The classification depends on factors like the device’s purpose, intended use, and potential risks, as outlined in FDA guidelines.
Why are some of Airlife’s devices reusable while others are single-use?
The reusability of a device depends on its design, risk level, and intended use. For example, reusable electrocardiographic lead sets are engineered to withstand repeated sterilization and use without compromising performance or patient safety. In contrast, single-use devices like anaesthesia breathing circuits or resuscitation kits are designed for one-time use to minimize infection risks and ensure consistent sterility, aligning with FDA’s risk-based classification approach.
AI-generated from registry data and not verified by a human reviewer.
Information
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- US
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Catalogue (2607)
Page 16 of 53| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| AirLife™ | 2K8050 | FDA UDI | Class I | Active |
| AirLife™ | 5424BDG1 | FDA UDI | Class II | Active |
| Vital Signs™ | A4UX2044 | FDA UDI | Class II | Active |
| Vital Signs™ | GASMXXXX | FDA UDI | Class I | Active |
| AirLife™ | 9007B | FDA UDI | Class II | Active |
| AirLife™ | FN2455 | FDA UDI | Class II | Active |
| AirLife™ | T262C | FDA UDI | Class I | Active |
| AirLife™ | 003005 | FDA UDI | Class I | Active |
| AirLife™ | 4000LRH | FDA UDI | Class I | Active |
| Multi-LinkTM | 2090600-038 | FDA UDI | Class II | Active |
| Vital Signs™ | IN900048 | FDA UDI | Class I | Active |
| Vital Signs™ | 5240 | FDA UDI | Class I | Active |
| Vital Signs™ | 4513VS | FDA UDI | Class I | Active |
| AirLife™ | 001013 | FDA UDI | Class I | Active |
| Vital Signs™ | 8040C | FDA UDI | Class II | Unknown |
| Vital Signs Breathing Bag | 1410008 | FDA UDI | Class I | Active |
| Vital Signs™ | A4UX2XXZU | FDA UDI | Class I | Active |
| Vital Signs™ | 6800EU | FDA UDI | Class I | Active |
| Vital Signs™ | A4Z12024 | FDA UDI | Class II | Active |
| Vital Signs™ | AFNX7904 | FDA UDI | Class I | Active |
| Multi-Link™ | 421930-003 | FDA UDI | Class II | Active |
| AirLife™ | K20 | FDA UDI | Class I | Active |
| Vital Signs™ | A41119X4 | FDA UDI | Class II | Active |
| Multi-Link™ | 1442AAO | FDA UDI | Class II | Active |
| Vital Signs™ | AGNX204X | FDA UDI | Class I | Active |
| AirLife™ | SFT2614 | FDA UDI | Class II | Active |
| AirLife™ | 10281-855 | FDA UDI | Class II | Active |
| Vital Signs™ | A5G529X4 | FDA UDI | Class I | Active |
| GreenLight™ | 4604EU | FDA UDI | Class I | Active |
| Vital Signs™ | S1000NEU | FDA UDI | Class I | Active |
| Vital Signs™ | GXXXXX58 | FDA UDI | Class I | Active |
| Multi-Link™ | 411202-005 | FDA UDI | Class II | Active |
| Vital Signs™ | 4830VS | FDA UDI | Class I | Active |
| Vital Signs™ | G4UX2OX4A1XFXXXX | FDA UDI | Class I | Unknown |
| Vital Signs™ | 5372AE | FDA UDI | Class I | Active |
| AirLife™ | T164C | FDA UDI | Class I | Active |
| Multi-Link™ | 2090100-081 | FDA UDI | Class II | Active |
| Vital Signs™ | B8754XXX | FDA UDI | Class I | Active |
| Vital Signs™ | A9U521XX | FDA UDI | Class I | Active |
| AirLife™ | 2K8005C2 | FDA UDI | Class II | Active |
| Vital Signs™ | A5V527XX | FDA UDI | Class I | Active |
| AirLife™ | NIV043S | FDA UDI | Class II | Active |
| AirLife™ | 2812M10-25 | FDA UDI | Class II | Active |
| Vital Signs™ | A4JXOXXX | FDA UDI | Class I | Active |
| AirLife™ | RC6Y023034 | FDA UDI | Class II | Active |
| Vital Signs™ | 5101BVL1 | FDA UDI | Class I | Active |
| AirLife™ | FM2614 | FDA UDI | Class II | Active |
| Airlife™ Bubble Humidifier with 6 psi Pressure Relief Valve | 002006 | FDA UDI | Class II | Active |
| Vital Signs™ | A4FX20X4D | FDA UDI | Class II | Active |
| Vital Signs™ | B1554XX4 | FDA UDI | Class I | Active |
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