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Ultrasound Bronchoscope
FDA product code PSV · Class 2 · Radiology
13
Registered devices
5,860
Adverse events
2
Recalls
3
510(k) clearances
Devices with this code
EVIS EXERA II ULTRASONIC BRONCHOFIBERVIDEOSCOPE — OLYMPUS MEDICAL SYSTEMS CORP.EVIS EXERA II ULTRASONIC BRONCHOFIBERVIDEOSCOPE — OLYMPUS MEDICAL SYSTEMS CORP.ULTRASONIC CABLE — OLYMPUS MEDICAL SYSTEMS CORP.EVIS EXERA II ULTRASONIC BRONCHOFIBERVIDEOSCOPE — OLYMPUS MEDICAL SYSTEMS CORP.EVES EUS ULTRASOUND BRONCHOFIBERVIDEOSCOPE — OLYMPUS MEDICAL SYSTEMS CORP.US CONNECTOR CAP — OLYMPUS MEDICAL SYSTEMS CORP.EVIS EXERA II ULTRASONIC BRONCHOFIBERVIDEOSCOPE — OLYMPUS MEDICAL SYSTEMS CORP.ULTRASONIC CABLE — OLYMPUS MEDICAL SYSTEMS CORP.EVIS EXERA II ULTRASONIC BRONCHOFIBERVIDEOSCOPE — OLYMPUS MEDICAL SYSTEMS CORP.EVIS EXERA II ULTRASONIC BRONCHOFIBERVIDEOSCOPE — OLYMPUS MEDICAL SYSTEMS CORP.Ultrasonic cable — OLYMPUS MEDICAL SYSTEMS CORP.EVIS EXERA II ULTRASONIC BRONCHOFIBERVIDEOSCOPE — OLYMPUS MEDICAL SYSTEMS CORP.EVIS EXERA II ULTRASONIC BRONCHOFIBERVIDEOSCOPE — OLYMPUS MEDICAL SYSTEMS CORP.
Recent recalls
| Date | Firm | Reason |
|---|---|---|
| 2023-09-25 | Aizu Olympus Co., Ltd. | Channel air drying process was not validated, and that a small percentage of scopes returned to customers after repair had a wet channel. Water remaining in the |
| 2023-07-27 | Olympus Corporation of the Americas | Complaint of endoscope model becoming lodged in the endotracheal tube connector due to diameter being too large. |
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