Home › Zoll Medical Corporation › M SERIES BIPHASIC
M SERIES BIPHASIC
Zoll Medical Corporation · Model 60021311110103010 · UDI-DI 00847946014179
4
510(k) clearances
16
Adverse events
6
Recalls
2
Facilities
Description
Defibrillator ,MAIN,BASIC-4,12LEAD,ETCO2,SPO2,BLUETOOTH,BIPHASIC,AC,PC,EL,RCD,SMR,CDMK,ENG,REFURB
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2005-06-08 | Boston Scientific Corporation | Potential for port housing separation after implantation. |
| 2005-06-08 | Boston Scientific Corporation | Potential for port housing separation after implantation. |
| 2005-06-08 | Boston Scientific Corporation | Potential for port housing separation after implantation. |
| 2005-02-25 | Boston Scientific Corporation | Potential separation of the port base from the port cover after implantation. |
| 2005-02-25 | Boston Scientific Corporation | Potential separation of the port base from the port cover after implantation. |
| 2005-02-25 | Boston Scientific Corporation | Potential separation of the port base from the port cover after implantation. |
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 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.