Home › Device types › BZB
Catheter, Nasal, Oxygen
FDA product code BZB · Class 1 · Anesthesiology
14
Registered devices
25
Adverse events
1
Recalls
8
510(k) clearances
Devices with this code
HUDSON RCI — TELEFLEX INCORPORATEDHUDSON RCI — TELEFLEX INCORPORATEDSHENGJIE — Weihai Shengjie Medical Technology Co., Ltd.SHENGJIE — Weihai Shengjie Medical Technology Co., Ltd.SHENGJIE — Weihai Shengjie Medical Technology Co., Ltd.SHENGJIE — Weihai Shengjie Medical Technology Co., Ltd.SHENGJIE — Weihai Shengjie Medical Technology Co., Ltd.SHENGJIE — Weihai Shengjie Medical Technology Co., Ltd.HUDSON RCI — TELEFLEX INCORPORATEDSHENGJIE — Weihai Shengjie Medical Technology Co., Ltd.SHENGJIE — Weihai Shengjie Medical Technology Co., Ltd.SHENGJIE — Weihai Shengjie Medical Technology Co., Ltd.HUDSON RCI — TELEFLEX INCORPORATEDSHENGJIE — Weihai Shengjie Medical Technology Co., Ltd.
Recent recalls
| Date | Firm | Reason |
|---|---|---|
| 2024-11-27 | 3B Medical, Inc. | The devices were inadvertently shipped after their expiration date. |
Query this across every FDA database — by API.
Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.
Get your free API keyRead the docsSourced from public U.S. FDA data. Informational only — not medical or regulatory advice. Not affiliated with the FDA.
