Hersill Sl
Country not established
Hersill Sl is a medical device manufacturer, with 36 devices listed in FDA GUDID (FDA Class II) as of 14 Nov 2026.
- Devices
- 36
Registry facts
- Registries
- FDA GUDID 36
- Device classes
- FDA Class II 36
- Identifiers
- DUNS 462032145
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.
Catalogue
Search and filter all 36 devicesCompany details
- DUNS number
- 462032145
Frequently asked questions
How many devices does HERSILL SL have in the registry?
The registry currently lists 36 devices for HERSILL SL. Devices recorded under merged duplicate company entries are counted once.
Which registries list HERSILL SL's devices?
Among its 36 most recently registered devices, HERSILL SL has devices listed in FDA GUDID (36 devices).
What risk classes do HERSILL SL's devices fall under?
Among its 36 most recently registered devices, the classes recorded for HERSILL SL's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from HERSILL SL in the registry?
The most recently registered devices listed for HERSILL SL include TITANIUM VAC REG CONT/INT DHDM, TITANIUM VAC REG PED CONT/INT CMDM, TITANIUM VAC REG CONT/INT OMBB and TITANIUM VAC REG MED VAC DHLG.