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Sign in to claim this brandSalter Labs, LLC
United States·US-MF-000007934
Last updated September 17, 2026
About
Anesthesia and respiratory care products. Humidity Delivered Just Right Explore DuoTherm® Humidification System for personalized, accurate patient care Learn MoreSeven Days, One Simplified SolutionExplore NEW BALLARD™ 7Day Closed Suction System Learn MoreNew Distribution Partnership Now partnering with Asker Healthcare to better serve customers in the UK, France, and GermanyReady for Any Intubation Extensive endotracheal tube portfolio \[…\]
From the manufacturer's own website. Source
What Salter Labs, LLC makes
Salter Labs, LLC manufactures nasal cannulas for adult patients, including a standard 14-foot supply tube and a divided cannula designed for simultaneous ETCO₂/O₂ delivery with female luer and thread grip connectors. The company also produces disposable pressure infusors, such as the InfuseIT 500 ml model, for controlled fluid administration.
These devices fall under Class IIa regulatory classification and are listed in the EU’s eudamed database. The manufacturer 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 Salter Labs, LLC manufacture?
Salter Labs, LLC specializes in devices for anesthesia and respiratory care. Their portfolio includes nasal cannulas for adult patients, such as a standard 14-foot supply tube and a divided cannula designed for combined ETCO₂ and oxygen delivery. They also produce disposable pressure infusors, like the InfuseIT 500 ml model, which are used for controlled fluid administration in clinical settings.
Where is Salter Labs, LLC based?
Salter Labs, LLC is headquartered in the United States. The company’s location is relevant for understanding its regulatory jurisdiction and compliance framework, particularly for devices marketed globally.
Which regulatory registries list Salter Labs, LLC’s devices?
Salter Labs, LLC’s devices are listed in the eudamed database, which is the European Union’s central registry for medical devices. This inclusion helps ensure transparency and traceability for devices marketed within the EU, aligning with their Class IIa classification.
How are Salter Labs, LLC’s devices classified under medical device regulations?
Salter Labs, LLC’s devices fall under Class IIa regulatory classification. This classification typically applies to devices with a lower risk profile but still require compliance with specific design controls, manufacturing processes, and post-market surveillance to ensure safety and performance.
AI-generated from registry data and not verified by a human reviewer.
Information
- Country
- United States
- Address
- 30, Spur Drive, El Paso, United States
- Website
- myairlife.com
- linkedin.com/company/myairlife
- facebook.com/profile.php
- [email protected]
- Phone
- +1-269-873-0502
- PRRC Contact
- Robert Yamashita
- EUDAMED SRN
- US-MF-000007934
- FDA FEI Number
- —
- DUNS Number
- —
Catalogue (39)
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