Home › Device types › NNY
Sheath, Corrugated Rubber, For Non-Indwelling Catheter, Non-Sterile
FDA product code NNY · Class 1 · Gastroenterology, Urology
17
Registered devices
0
Adverse events
3
Recalls
0
510(k) clearances
Devices with this code
RUSCH — TELEFLEX INCORPORATEDRUSCH — TELEFLEX INCORPORATEDRUSCH — TELEFLEX INCORPORATEDRUSCH — TELEFLEX INCORPORATEDRUSCH — TELEFLEX INCORPORATEDRUSCH — TELEFLEX INCORPORATEDRUSCH — TELEFLEX INCORPORATEDAcanthus — Acanthus Medical Creations LLCRUSCH — TELEFLEX INCORPORATEDRUSCH — TELEFLEX INCORPORATEDRUSCH — TELEFLEX INCORPORATEDAcanthus — Acanthus Medical Creations LLCRUSCH — TELEFLEX INCORPORATEDRUSCH — TELEFLEX INCORPORATEDRUSCH — TELEFLEX INCORPORATEDRUSCH — TELEFLEX INCORPORATEDRUSCH — TELEFLEX INCORPORATED
Recent recalls
| Date | Firm | Reason |
|---|---|---|
| 2019-02-27 | Teleflex Medical | The device label incorrectly states that the device is sterile. This product is an externally applied male condom-type catheter designed for the management of m |
| 2019-02-27 | Teleflex Medical | The device label incorrectly states that the device is sterile. This product is an externally applied male condom-type catheter designed for the management of m |
| 2011-06-27 | Teleflex Medical | The Kit contains Skin-Prep protective wipes that were manufactured by the Triad Group and are being recalled by Smith & Nephew, due to possible bacterial contam |
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