Bard® Foley Tray With Hydrophilic-Coated Foley Catheter

6 catalogue numbers from 861016, listed by C.R. Bard, Inc., United States, under Catheter, Coude. 1 manufacturer in China is registered for this product code.

Registry build 21.09.26
1manufacturer
6catalogue 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.

Chinese manufacturers registered for FDA product code EZC
Manufacturer City Province Registered as Device types
Jiangsu Suyun Medical Materials Co., Ltd. Lianyungang Jiangsu Contract manufacturer 11

Record

Regulatory record for Bard® Foley Tray with Hydrophilic-Coated Foley Catheter
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

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 14 to 18 Fr

Catalogue Numbers

Catalogue numbers for Bard® Foley Tray with Hydrophilic-Coated Foley Catheter
Catalogue number Size Status
861016 Catheter Gauge 16 Fr In distribution
861416 Catheter Gauge 16 Fr In distribution
861418 Catheter Gauge 18 Fr In distribution
861014 Catheter Gauge 14 Fr In distribution
861018 Catheter Gauge 18 Fr In distribution
861414 Catheter Gauge 14 Fr In distribution

Same Product Code

Showing 12 of 66. All products under Catheter, Coude

510(K) Clearances

FDA 510(k) clearances naming this product code
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.

Recalls referencing this product code
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.

Where China Actually Supplies

Every device page names the company that lists it and the factories registered to make the same thing. These are the sections with the most of them.

5,100manufacturers registered in China
2,581device types they are registered for
340,248device records, each naming its maker
31provinces with a registered manufacturer