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Ambu
Technomed Engineering B.V. · Model 75021-150/25 · UDI-DI 08718375869154
10
510(k) clearances
150
Adverse events
2
Recalls
39
Facilities
Description
Ambu ® Subdermal Curved Needle, 1.5m wire 5x5 colors 25pcs, disposable
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2022-08-09 | Technomed Europe | Burns of varying degrees can occur to patients with electrodes left in while in the MRI scanner as a result of inadequate safety information in the IFU. |
| 2007-04-12 | Chalgren Enterprises Inc | Sterility Compromised-- Investigation found that individual packaging seals were separating, which may compromise sterility. |
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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.