Device, Incontinence, Urosheath Type, Non-sterile
C.r. Bard, Inc.'s record for this product code
MDR events841All time
Recalls0All time
510(k) clearances0All time
Recent MDR events
841 adverse event reports on file
- UNKNOWN MALE EXTERNAL CATHETERNov 19, 2025Injury1018233-2025-10382
- UNKNOWN MALE EXTERNAL CATHETERNov 19, 2025Injury1018233-2025-10384
- UNKNOWN MALE EXTERNAL CATHETERNov 19, 2025Injury1018233-2025-10383
- WIDEBAND¿ SELF-ADHERING MALE EXTERNAL CATHETERNov 10, 2025Injury1018233-2025-10144
- UNKNOWN MALE EXTERNAL CATHETEROct 27, 2025Injury1018233-2025-09594
- WIDEBAND¿ SELF-ADHERING MALE EXTERNAL CATHETERSep 17, 2025Injury1018233-2025-08253
- MALE EXTERNAL CATHETERSep 3, 2025Injury1018233-2025-07430
- SPIRIT® HYDROCOLLOID ADHESIVE SHEATHAug 25, 2025Injury1018233-2025-07005
- WIDEBAND¿ SELF-ADHERING MALE EXTERNAL CATHETERAug 15, 2025Injury1018233-2025-06810
- WIDEBAND¿ SELF-ADHERING MALE EXTERNAL CATHETERJul 31, 2025Injury1018233-2025-06329
Recalls
0 recall events for this product code
No recalls on file for C.r. Bard, Inc. under this product code.
510(k) clearances
0 clearances for this product code
No 510(k) clearances on file for C.r. Bard, Inc. under this product code.