Bard® Foley Catheter Tray With Bard® Hydrophilic-Coated Foley Catheter
2 catalogue numbers from 800066, listed by C.R. Bard, Inc., United States, under Catheter, Coude. 1 manufacturer in China is registered for this product code.
Who Else Makes It
Registered in Jiangsu. One is registered as a contract manufacturer, able to build to a specification.
| Manufacturer | City | Province | Registered as | Device types |
|---|---|---|---|---|
| Jiangsu Suyun Medical Materials Co., Ltd. | Lianyungang | Jiangsu | Contract manufacturer | 11 |
Record
| Listed by | C.R. Bard, Inc., United States |
|---|---|
| FDA product code | EZC |
| Device type | Catheter, Coude |
| Device class | Class 2 |
| Regulation | 21 CFR 876.5130 |
| Establishment | Contract manufacturer, Contract steriliser, Specification developer, Repacker / relabeller, Complaint-file establishment, Manufacturer, Exporter |
| Record published | 2016-07-28 |
| Record revised | 2020-12-04 (version 3) |
Specifications
| MRI safety | Labeling does not contain MRI Safety Information |
|---|---|
| Supplied sterile | Yes |
| Single use | Yes |
| Prescription | Prescription only |
| Supplied as a kit | Yes |
| Latex | Contains natural rubber latex |
| Label carries | lot or batch number, expiry date |
| Packaging | Case of 10 |
| Sizes | Catheter gauge 16 to 18 Fr |
Catalogue Numbers
| Catalogue number | Size | Status |
|---|---|---|
| 800066 | Catheter Gauge 18 Fr | In distribution |
| 800065 | Catheter Gauge 16 Fr | In distribution |
Same Product Code
| Product | Sold by | Catalogue numbers |
|---|---|---|
| Bardex® Lubricath® Foley Catheter | C.R. Bard, Inc. | 26 |
| SureStep™ Foley Tray System Bard® Lubricath® Foley Catheter Tray | C.R. Bard, Inc. | 18 |
| Rusch | Teleflex Medical LLC | 14 |
| SureStep™ Foley Tray System Bardex® Lubricath® Foley Catheter | C.R. Bard, Inc. | 12 |
| Bard® Urine Meter Foley Tray with Bardex® Lubricath® Foley Catheter | C.R. Bard, Inc. | 11 |
| Bardex® Silicone Coated Foley Catheter | C.R. Bard, Inc. | 10 |
| Bardia | C.R. Bard, Inc. | 10 |
| Bardia® Foley Catheter Silicone Coated | C.R. Bard, Inc. | 10 |
| Bard® Foley Catheter Silicone Coated | C.R. Bard, Inc. | 10 |
| Bard® Lubricath® Foley Catheter | C.R. Bard, Inc. | 10 |
| Bardex® Silicone Elastomer-Coated Foley Catheter Kit | C.R. Bard, Inc. | 8 |
| Bardex® Lubricath® Hydrogel-Coated Foley Catheter Kit | C.R. Bard, Inc. | 8 |
Showing 12 of 66. All products under Catheter, Coude
510(K) Clearances
| Clearance | Decision date |
|---|---|
| K913341 | 1992-01-27 |
| K910846 | 1991-08-16 |
| K910197 | 1991-08-09 |
| K910195 | 1991-08-09 |
Recalls
10 of these are Class II. Class II means a temporary or reversible health consequence. Volume alone is not a quality signal: a manufacturer that ships more recalls more.
| Initiated | FDA class | Root cause | Reason | Quantity | Closed |
|---|---|---|---|---|---|
| 2026-06-25 | Not classified | Under Investigation by firm | Due to complaints received indicating presence of contamination on the surface of pericare wipes provided with various Foley and Intermittent Catheter Trays. | 12,463 trays/kits | |
| 2025-06-03 | Class II | Under Investigation by firm | Cather packaging may contain the incorrect French size. | 63 units | |
| 2021-08-05 | Class II | Packaging change control | There is potential for packaging defects that may impact the sterile barrier. | 960 units | |
| 2021-08-05 | Class II | Packaging change control | There is potential for packaging defects that may impact the sterile barrier. | 2660 units | |
| 2021-08-05 | Class II | Packaging change control | There is potential for packaging defects that may impact the sterile barrier. | 18,060 units | |
| 2021-08-05 | Class II | Packaging change control | There is potential for packaging defects that may impact the sterile barrier. | 29,890 units | |
| 2021-08-05 | Class II | Packaging change control | There is potential for packaging defects that may impact the sterile barrier. | 33,380 units | |
| 2021-08-05 | Class II | Packaging change control | There is potential for packaging defects that may impact the sterile barrier. | 80 units | |
| 2021-08-05 | Class II | Packaging change control | There is potential for packaging defects that may impact the sterile barrier. | 1140 units | |
| 2017-12-13 | Class II | Process control | Foley Catheter with Incorrect Retainer Cap Print | 2020-12-14 | |
| 2012-06-29 | Class II | Process control | Incomplete seal on sterile packages of product. | 56,694 units | 2013-02-07 |
Source: U.S. FDA establishment registration and device listing records, public domain. Restructured for clarity and searchability. Not affiliated with or endorsed by the FDA. Records are records: nothing here is an offer of sale.