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Tubing/Tubing With Filter, Insufflation, Laparoscopic
FDA product code NKC · Class 1 · Obstetrics/Gynecology
257
Registered devices
51
Adverse events
3
Recalls
0
510(k) clearances
Devices with this code
DeRoyal — DEROYAL INDUSTRIES, INC.PMI — PROGRESSIVE MEDICAL, INC.JosNoe Medical Inc — JOSNOE MEDICAL, INC.n.a. — Karl Storz GmbH & Co. KGTubing, with filter, sterile, for insuflation — Promeplan.a. — Karl Storz GmbH & Co. KGTech-Medical Services — TECHMEDICAL SERVICES, INC.Medline Industries, Inc. — MEDLINE INDUSTRIES, INC.n.a. — Karl Storz GmbH & Co. KGDeRoyal — DEROYAL INDUSTRIES, INC.CHS — DEROYAL INDUSTRIES, INC.Buffalo Filter — Buffalo FilterDeRoyal — DEROYAL INDUSTRIES, INC.andorate® CO2 Source Tubing Adapter — GA Health Company LimitedJosNoe Medical Inc — JOSNOE MEDICAL, INC.DeRoyal — DEROYAL INDUSTRIES, INC.Surgical Direct — Surgical Direct, Inc.CARDINAL HEALTH — Cardinal Health 200, LLCHose for CO2 central gas supply AGA-US, 3 m — W.O.M. World of Medicine GmbHn.a. — Karl Storz GmbH & Co. KGDeRoyal — DEROYAL INDUSTRIES, INC.n.a. — Karl Storz GmbH & Co. KGDeRoyal — DEROYAL INDUSTRIES, INC.andorate® CO2 Source Tubing Adapter — GA Health Company Limited
Recent recalls
| Date | Firm | Reason |
|---|---|---|
| 2019-01-09 | Karl Storz Endoscopy | The sterile single-use tubing may contain higher ethylene oxide (EO) residues than the acceptable level. |
| 2017-10-10 | Karl Storz Endoscopy | The label outside the cardboard box is labeled correctly but the pouches inside of some of the boxes were mislabeled as a different product. |
| 2013-07-15 | DeRoyal Industries Inc | DeRoyal Industries is recalling their product Insufflation Tubing Sets due to materials incompatibility which could possibly result in occlusion at or near the |
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