Bausch + Lomb Ireland Limited
Country not established
- Devices
- 1
What Bausch + Lomb Ireland Limited makes
Bausch + Lomb Ireland Limited manufactures laser systems and slit lamp adapters designed for ophthalmic procedures, including the QuanteL Activis Laser and specialized adapters such as the ZSL30 ACT, ZSL120 ACT, and HSBMBQ ACT for slit lamps. These devices are intended for use in precision eye surgeries and diagnostic imaging within clinical settings.
The company’s portfolio is regulated under Class III medical devices in the United States, requiring Premarket Approval (PMA) through the FDA. These products are listed under the FDA’s PMA registry, reflecting their classification as high-risk devices requiring stringent pre-market evaluation. The manufacturer is based in the United States.
Catalogue
- Regimes: PMA Registry: PMA
Frequently asked questions
How many devices does Bausch + Lomb Ireland Limited have in the registry?
The registry currently lists 1 device for Bausch + Lomb Ireland Limited. Devices recorded under merged duplicate company entries are counted once.
Which registries list Bausch + Lomb Ireland Limited's devices?
Among its 1 most recently registered device, Bausch + Lomb Ireland Limited has devices listed in FDA PMA (1 device).
What risk classes do Bausch + Lomb Ireland Limited's devices fall under?
Among its 1 most recently registered device, the classes recorded for Bausch + Lomb Ireland Limited's devices are Class III. Each device page shows its own class and authorisation.
What are the newest devices from Bausch + Lomb Ireland Limited in the registry?
The most recently registered devices listed for Bausch + Lomb Ireland Limited include QUANTEL ACTIVIS LASER AND ZSL30 ACT, ZSL120 ACT, AND HSBMBQ ACT SLIT LAMP ADAPTERS.