Bardia
Bardia Silicone Elastomer Coated Foley Catheter
1manufacturer
10catalogue numbers in this listing
4510(k) clearances naming this product code
11recalls on this 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 | 2023-08-21 |
Specifications
| MRI safety | Labeling does not contain MRI Safety Information |
|---|---|
| Supplied sterile | Yes |
| Single use | Yes |
| Prescription | Prescription only |
| Latex | Contains natural rubber latex |
| Label carries | lot or batch number, expiry date |
| Storage | Special storage condition: Store catheters at room temperature away from direct exposure to light, preferably in the original box. |
| Packaging | Box of 10, case of 32 |
| Sizes | Catheter gauge 12 to 30 Fr; total volume 5 ml |
Catalogue Numbers
| Catalogue number | Size | Status |
|---|---|---|
| 123524CE | Catheter Gauge 24 Fr | In distribution |
| 123522CE | Total Volume 5 ml | In distribution |
| 123530CE | Total Volume 5 ml | In distribution |
| 123518CE | Total Volume 5 ml | In distribution |
| 123528CE | Total Volume 5 ml | In distribution |
| 123516CE | Total Volume 5 ml | In distribution |
| 123526CE | Total Volume 5 ml | In distribution |
| 123514CE | Catheter Gauge 14 Fr | In distribution |
| 123520CE | Total Volume 5 ml | In distribution |
| 123512CE | Catheter Gauge 12 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® 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 |
| Bard® Foley Tray with Bardex® Lubricath® Foley Catheter | 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.