Catheter, straight
FDA product code EZD · Class 2 · 125 devices · 3,071 reports · 3 deaths reported · 18 devices named in recalls
- Self-Cath 50462 / 212Coloplast A/S · CATHETER, STRAIGHT1 report
- LoFric® Sense™ 4161025Wellspect AB · Catheter, straight1 report
- LoFric® Elle™ 4181425Wellspect AB · Catheter, straight1 report
- LoFric® Elle™ 4181450Wellspect AB · Catheter, straight1 report
- GentleCath Hydrophilic 508996Wellspect AB · Catheter, straight1 report
- LoFric® 40014Wellspect AB · Catheter, straight1 report
- LoFric® Hydro-Kit™ 42010Wellspect AB · Catheter, straight1 report
- LoFric® Hydro-Kit™ 42018Wellspect AB · Catheter, straight1 report
- LoFric® Hydro-Kit™ 42516Wellspect AB · Catheter, straight1 report
- LoFric® Primo™ 41014Wellspect AB · Catheter, straight1 report
- LoFric® Primo™ 41312Wellspect AB · Catheter, straight1 report
- LoFric® Origo™ 44310Wellspect AB · Catheter, straight1 report
- LoFric® Origo™ 44316Wellspect AB · Catheter, straight1 report
- LoFric® Origo™ 44410Wellspect AB · Catheter, straight1 report
- LoFric® Sense™ 4161250Wellspect AB · CATHETER, STRAIGHT1 report
- LoFric® Origo™ 44316Wellspect AB · CATHETER, STRAIGHT1 report
- LoFric® Origo™ 44414Wellspect AB · CATHETER, STRAIGHT1 report
- LoFric® 40512Wellspect AB · CATHETER, STRAIGHT1 report
- LoFric® 40018Wellspect AB · CATHETER, STRAIGHT1 report
- LoFric® 40314Wellspect AB · CATHETER, STRAIGHT1 report
- LoFric® Hydro-Kit™ 42312Wellspect AB · CATHETER, STRAIGHT1 report
- LoFric® Hydro-Kit™ 42514Wellspect AB · CATHETER, STRAIGHT1 report
- hi-slip® plus HS.PM4014Oasis Medikal Urunler Kimya Turizm Sanayi Ve Ticaret Anonim Sirketi · CATHETER, STRAIGHT1 report
- Medline DYND10702Medline Industries, Inc. · CATHETER, STRAIGHT1 report
- Medline DYND10723Medline Industries, Inc. · CATHETER, STRAIGHT1 report