Eschmann Bros. & Walsh, Ltd.
Country not established
- Devices
- 3
What Eschmann Bros. & Walsh, Ltd. makes
Eschmann Bros. & Walsh, Ltd. manufactures electrosurgical units, including the Model TD411, and specialized medical devices such as modified dilatation catheters and a device for treating female incontinence. These products are designed for surgical and procedural applications requiring precise control and targeted interventions.
The company’s portfolio is regulated under Class II medical devices in the US, with relevant products listed via the FDA’s 510(k) pathway. The devices are intended for commercial distribution within the United States.
Catalogue
Eschmann Electrosurgical Unit, Model TD411 Ref K852935
Regimes: 510(k) Registry: 510(k)Modified Eschmann Dilatation Catheter Ref K864637
Regimes: 510(k) Registry: 510(k)Device, Female Incontinence Ref K781863
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Eschmann Bros. & Walsh, Ltd. have in the registry?
The registry currently lists 3 devices for Eschmann Bros. & Walsh, Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Eschmann Bros. & Walsh, Ltd.'s devices?
Among its 3 most recently registered devices, Eschmann Bros. & Walsh, Ltd. has devices listed in FDA 510(k) (3 devices).
What risk classes do Eschmann Bros. & Walsh, Ltd.'s devices fall under?
Among its 3 most recently registered devices, the classes recorded for Eschmann Bros. & Walsh, Ltd.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Eschmann Bros. & Walsh, Ltd. in the registry?
The most recently registered devices listed for Eschmann Bros. & Walsh, Ltd. include ESCHMANN ELECTROSURGICAL UNIT, MODEL TD411, MODIFIED ESCHMANN DILATATION CATHETER and DEVICE, FEMALE INCONTINENCE.