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SHENGJIE
Weihai Shengjie Medical Technology Co., Ltd. · Model M1 · UDI-DI 06970614670347
8
510(k) clearances
25
Adverse events (1 deaths)
1
Recalls
36
Facilities
Description
Oxygen Tube
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2024-11-27 | 3B Medical, Inc. | The devices were inadvertently shipped after their expiration date. |
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Get your free API keyRead the docsData compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.