Home › Device types › MOD
Accessory To Continuous Ventilator (Respirator)
FDA product code MOD · Class 2 · Anesthesiology
111
Registered devices
19
Adverse events
2
Recalls
16
510(k) clearances
Devices with this code
Bio-Med Devices, Inc. — BIO-MED DEVICES, INC.Bio-Med Devices, Inc. — BIO-MED DEVICES, INC.Bio-Med Devices, Inc. — BIO-MED DEVICES, INC.Bio-Med Devices, Inc. — BIO-MED DEVICES, INC.Bio-Med Devices, Inc. — BIO-MED DEVICES, INC.Tyco-Achieva Bulk — GVS FILTER TECHNOLOGY UK LTDBio-Med Devices, Inc. — BIO-MED DEVICES, INC.Bio-Med Devices, Inc. — BIO-MED DEVICES, INC.Bio-Med Devices, Inc. — BIO-MED DEVICES, INC.Bio-Med Devices, Inc. — BIO-MED DEVICES, INC.Bio-Med Devices, Inc. — BIO-MED DEVICES, INC.Bio-Med Devices, Inc. — BIO-MED DEVICES, INC.Bio-Med Devices, Inc. — BIO-MED DEVICES, INC.Bio-Med Devices, Inc. — BIO-MED DEVICES, INC.Bio-Med Devices, Inc. — BIO-MED DEVICES, INC.Bio-Med Devices, Inc. — BIO-MED DEVICES, INC.Cart, Display Enclosure 11 inch — CORVENT MEDICAL, INCCorVent® CorVision — CORVENT MEDICAL, INCBio-Med Devices, Inc. — BIO-MED DEVICES, INC.Bio-Med Devices, Inc. — BIO-MED DEVICES, INC.Bio-Med Devices, Inc. — BIO-MED DEVICES, INC.Bio-Med Devices, Inc. — BIO-MED DEVICES, INC.Bio-Med Devices, Inc. — BIO-MED DEVICES, INC.Bio-Med Devices, Inc. — BIO-MED DEVICES, INC.
Recent recalls
| Date | Firm | Reason |
|---|---|---|
| 2026-08-18 | Percussionaire Corporation | Labeling updated warning not to use Intrapulmonary percussive ventilation (IPV) in conjunction with volatile anesthetic delivery systems because IPV may alter c |
| 2005-06-08 | Medical Device Group Inc. | Device separation presenting a choking hazard. |
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