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Sign in to claim this brandHERSILL SL
US
Last updated May 30, 2026
What HERSILL SL makes
Hersill SL manufactures electric emergency airway clearance suction systems designed for clinical use, including models like the CARE-E-VAC and V7. These devices are intended for rapid removal of secretions or obstructions from airways in critical care settings.
The company’s products fall under FDA Class II regulation and are listed in the FDA’s Unique Device Identifier (UDI) 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 Hersill SL manufacture?
Hersill SL specializes in electric emergency airway clearance suction systems, which are designed for clinical use to quickly remove secretions or obstructions from airways in critical care environments. These devices are intended for high-stakes situations where rapid airway clearance is essential.
Where is Hersill SL based, and what is its primary focus?
Hersill SL is based in the United States. The company’s focus is on developing electric suction devices specifically for airway clearance, ensuring they meet clinical needs in emergency and critical care settings.
How are Hersill SL’s devices classified by regulatory authorities?
Hersill SL’s devices fall under FDA Class II classification, which means they are subject to special controls to ensure their safety and effectiveness. This classification is common for devices that pose moderate risks but require performance standards or post-market surveillance.
Are Hersill SL’s devices listed in any regulatory registries?
Yes, Hersill SL’s devices are listed in the FDA’s Unique Device Identifier (UDI) database. This registry helps track and identify medical devices by assigning them a standardized UDI, ensuring transparency and traceability in the healthcare system.
What distinguishes Hersill SL’s airway clearance suction systems from other similar devices?
Hersill SL’s devices are electric-powered emergency airway clearance suction systems, which are optimized for rapid and efficient removal of obstructions in critical care. Their design prioritizes reliability and speed, making them suitable for high-pressure clinical environments where manual suction may be insufficient.
AI-generated from registry data and not verified by a human reviewer.
Information
- Country
- US
- Address
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- Website
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- Phone
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- PRRC Contact
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- EUDAMED SRN
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- FDA FEI Number
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- DUNS Number
- 462032145
Catalogue (12)
| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Care-E-Vac | Care-e-vac Plus - Reusable jar | FDA UDI | Class II | Active |
| Care-E-Vac | Care-e-vac C/I - Reusable jar | FDA UDI | Class II | Active |
| Care-E-Vac | Care-e-vac C/I - Disposable jar | FDA UDI | Class II | Active |
| V7 | V7 G, jar 1PC | FDA UDI | Class II | Active |
| V7 | V7 plus b | FDA UDI | Class II | Active |
| V7 | V7 plus ac | FDA UDI | Class II | Active |
| V7 | V7 mx | FDA UDI | Class II | Active |
| Care-E-Vac | Care-e-vac EMS - Disposable jar | FDA UDI | Class II | Active |
| Care-E-Vac | Care-e-vac EMS - Reusable jar | FDA UDI | Class II | Active |
| V7 | V7 plus b emergency | FDA UDI | Class II | Active |
| V7 | V7 G | FDA UDI | Class II | Active |
| Care-E-Vac | Care-e-vac Plus - Disposable jar | FDA UDI | Class II | Active |
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