# C.R. Bard, Inc. (contract sterilizer, Covington, GA): 11 new FDA device listings, incl. plethysmograph, impedance

**Score:** 90/100

| Field | Value |
|---|---|
| Establishment | C.R. Bard, Inc. |
| Owner / operator | C. R. Bard, Inc. |
| Role | Contract sterilizer |
| Establishment types | Sterilize Medical Device for Another Party (Contract Sterilizer); Develop Specifications But Do Not Manufacture At This Facility |
| Location | Covington, GA, US |
| New listings | 11 |
| Devices | Plethysmograph, Impedance; Transducer, Blood-Pressure, Extravascular; Catheter, Continuous Flush; Transducer, Pressure, Catheter Tip; Tray, Catheterization, Sterile Urethral, With Or Without Catheter (Kit); Probe, Thermodilution; Catheter, Flow Directed; Tubes, Gastrointestinal (And Accessories); Catheter, Oximeter, Fiber-Optic; Introducer, Catheter |
| Product codes | DSB, DRS, KRA, DXO, FCM, KRB, DYG, KNT, DQE, DYB, LDF |
| Device classes | Class II |
| Medical specialties | Cardiovascular, Gastroenterology, Urology |
| Brand names | ClearSight and AcumenIQ finger cuffs; FloTrac Sensor; VAMP Venous/Arterial Blood Management Protection System; TruWave™ Disposable Pressure Transducers; Unisex Pre-Lubricated Urethral Catheter Kit, Rubber Urethral Catheter; CO-SET; Swan Ganz Catheters; Blakemore Esophageal-Nasogastric Tube |
| First new listing | 2026-05-28 |
| Latest new listing | 2026-09-23 |
| FDA registration number | 1018233 |
| Registration expires | 2027-12-31 |

## Why this score
- Contract manufacturer or sterilizer adding work.
- Class II or III devices: QMS and regulatory demands.
- Several new listings at once.
- U.S. establishment.
- Listed in the last 45 days.

Source: openFDA device registration and listing endpoint (U.S. Food and Drug Administration) (https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRL/rl.cfm). Last refreshed: 2026-10-28T20:51:27.468Z.
From the openFDA device registration and listing data, refreshed weekly. A listing shows a device an establishment says it makes or handles for the U.S. market; it is not FDA clearance or approval. Contact persons and street addresses are not stored. Verify in the FDA Establishment Registration and Device Listing database.