Home › Device types › EYB
Catheter, Ureteral, Gastro-Urology
FDA product code EYB · Class 2 · Gastroenterology, Urology
268
Registered devices
354
Adverse events
4
Recalls
28
510(k) clearances
Devices with this code
Coloplast — Coloplast A/SSof-Flex — COOK INCORPORATEDPorges Coloplast — Coloplast A/STruCath — HR PHARMACEUTICALS INC.Bard® Woven Ureteral Catheter — C. R. Bard, Inc.MEDLINE — MEDLINE INDUSTRIES, INC.TruCath — HR PHARMACEUTICALS INC.Bard® Woven Ureteral Catheter — C. R. Bard, Inc.Coloplast — Coloplast A/SPorges Coloplast — Coloplast A/SPorges Coloplast — Coloplast A/SColoplast — Coloplast A/SNA — Richard Wolf GmbHBard® Polyurethane Ureteral Catheters, Cone Tip — C. R. Bard, Inc.Coloplast — Coloplast A/SBard® Woven Ureteral Catheter — C. R. Bard, Inc.Porges Coloplast — Coloplast A/SMEDLINE — MEDLINE INDUSTRIES, INC.AMSure® Red Rubber Urethral Catheter — AMSINO INTERNATIONAL, INC.MEDLINE — MEDLINE INDUSTRIES, INC.Coloplast — Coloplast A/SBard® Polyurethane Ureteral Catheters, Open Tip — C. R. Bard, Inc.Red Rubber Urethral Catheters — Dynarex CorporationBard® Polyurethane Ureteral Catheters, Open Tip — C. R. Bard, Inc.
Recent recalls
| Date | Firm | Reason |
|---|---|---|
| 2026-05-04 | Medline Industries, LP | During an internal review, Medline identified representative samples did not meet applicable performance specifications. Identified issues include irregularitie |
| 2026-05-04 | Medline Industries, LP | During an internal review, Medline identified representative samples did not meet applicable performance specifications. Identified issues include irregularitie |
| 2022-07-29 | Hobbs Medical, Inc. | Device label display an incorrect expiration date, extends the shelf life of the product. Affected product distributed in the United States from 3/25/2018 to 9 |
| 2008-06-25 | Gyrus ACMI Corporation | Particulate matter in the catheter |
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