Home › Device types › DWQ
Stripper, Vein, External
FDA product code DWQ · Class 2 · Cardiovascular
15
Registered devices
106
Adverse events
2
Recalls
8
510(k) clearances
Devices with this code
Trivex System — Lemaitre Vascular, Inc.Trivex System — Lemaitre Vascular, Inc.Trivex System — Lemaitre Vascular, Inc.Trivex System — Lemaitre Vascular, Inc.Trivex System — Lemaitre Vascular, Inc.Trivex System — Lemaitre Vascular, Inc.Trivex System — Lemaitre Vascular, Inc.Trivex System — Lemaitre Vascular, Inc.Trivex System — Lemaitre Vascular, Inc.Trivex System — Lemaitre Vascular, Inc.Trivex System — Lemaitre Vascular, Inc.Trivex System — Lemaitre Vascular, Inc.Trivex System — Lemaitre Vascular, Inc.Trivex System — Lemaitre Vascular, Inc.Trivex System — Lemaitre Vascular, Inc.
Recent recalls
| Date | Firm | Reason |
|---|---|---|
| 2015-02-24 | LeMaitre Vascular, Inc. | Mislabeled with an incorrect expiration date |
| 2004-10-12 | Smith & Nephew, Inc Endoscopy Division | Build-up of static charge in Pneumatic Footswitch tubing may cause control unit to reset to default settings in the operating room during surgery. |
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