Creagh Medical Ltd. Dba Surmodics, Inc.
IrelandFDA 510(k) applicant, unverified
- Devices
- 1
Catalogue
What Creagh Medical Ltd. Dba Surmodics, Inc. makes
Creagh Medical Ltd. (dba Surmodics, Inc.) manufactures the 018 Hydrophilic Coated Over-The-Wire (OTW) Percutaneous Transluminal Angioplasty (PTA) Balloon Dilatation Catheter, a device designed for vascular dilation in interventional procedures.
This product is classified as Class II under FDA regulations and is listed via 510(k) clearance. The company is headquartered in the United States.
Frequently asked questions
How many devices does Creagh Medical Ltd. Dba Surmodics, Inc. have in the registry?
The registry currently lists 1 device for Creagh Medical Ltd. Dba Surmodics, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Creagh Medical Ltd. Dba Surmodics, Inc.'s devices?
Among its 1 most recently registered device, Creagh Medical Ltd. Dba Surmodics, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Creagh Medical Ltd. Dba Surmodics, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Creagh Medical Ltd. Dba Surmodics, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Creagh Medical Ltd. Dba Surmodics, Inc. in the registry?
The most recently registered devices listed for Creagh Medical Ltd. Dba Surmodics, Inc. include 018 Hydrophilic Coated OTW PTA Balloon Dilatation Catheter.