Usci, Div. C.R. Bard, Inc.
United StatesFDA applicant, unverified
- Devices
- 13
What Usci, Div. C.R. Bard, Inc. makes
Usci manufactures vascular access and cardiovascular devices, including percutaneous introducers and sheaths, cardiovascular catheters, and vascular prostheses such as filamentous prostheses, transparent manifolds, and bifurcated grafts. Their portfolio also covers infusion and probing catheters, arterial/venous introducers, vascular patch fabrics, and temporary atrial electrode kits, along with stainless steel safety spring guides for procedural support.
These devices are classified under FDA Class II regulations and are authorised via 510(k) and PMA pathways. The manufacturer is based in the United States and its products are listed in the FDA’s 510(k) and PMA registries.
Catalogue
Search and filter all 13 devicesFrequently asked questions
How many devices does Usci, Div. C.R. Bard, Inc. have in the registry?
The registry currently lists 13 devices for Usci, Div. C.R. Bard, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Usci, Div. C.R. Bard, Inc.'s devices?
Among its 13 most recently registered devices, Usci, Div. C.R. Bard, Inc. has devices listed in FDA 510(k) (12 devices) and FDA PMA (1 device). A device can be listed in more than one registry, so these counts overlap.
What risk classes do Usci, Div. C.R. Bard, Inc.'s devices fall under?
Among its 13 most recently registered devices, the classes recorded for Usci, Div. C.R. Bard, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Usci, Div. C.R. Bard, Inc. in the registry?
The most recently registered devices listed for Usci, Div. C.R. Bard, Inc. include CATHETER, PERCUTANEOUS INTRODUC. & SHEATH, CATHETER, CARDIOVASCULAR, SAUVAGE FILAMENTOUS PROSTHESES and PALEY TRANSPARENT MANIFOLD.