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Eicken antrum cannula
Spiggle & Theis Medizintechnik GmbH · Model 30-090-40 · UDI-DI 04250676712486
KAM
Prescription
10
510(k) clearances
61
Adverse events (1 deaths)
2
Recalls
56
Facilities
Description
long curve, Ø 4.0 mm bendable, with suction control
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2015-04-28 | Acclarent, Inc. | Acclarent determined that one single RELIEVA FLEX Sinus Guide Catheter was distributed past it's expiry date. |
| 2013-05-03 | Surgical Instrument Service And Savings, Inc. | The seal which maintains a sterile barrier for reprocessed medical devices became compromised to the point where product may fall out of the pouch. |
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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.
