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Tianjin Medis Medical Device Co.,Ltd. · Model NF204 · UDI-DI 06920687300207
10
510(k) clearances
313
Adverse events (3 deaths)
2
Recalls
127
Facilities
Description
with O2 Port, RespiratoryIndicator, Filter, Soft Tip and 15mm Connector 4.0mm
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2024-07-18 | Smiths Medical ASD Inc. | Uncertainty in the seal integrity of the sterile packaging. |
| 2017-01-13 | Teleflex Medical | Labeling error |
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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.