All the vulnerabilites related to Philips - IntelliVue X3
var-202009-0595
Vulnerability from variot

In Patient Information Center iX (PICiX) Versions C.02 and C.03, PerformanceBridge Focal Point Version A.01, IntelliVue patient monitors MX100, MX400-MX550, MX750, MX850, and IntelliVue X3 Versions N and prior, the software does not check or incorrectly checks the revocation status of a certificate, which may cause it to use a compromised certificate. A vulnerability exists in Patient Information. The vulnerability stems from special elements that may be interpreted as commands when spreadsheet software opens the file. The following products and versions are affected: B.02, C.02, C.03

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var-202009-0604
Vulnerability from variot

In IntelliVue patient monitors MX100, MX400-550, MX600, MX700, MX750, MX800, MX850, MP2-MP90, and IntelliVue X2 and X3 Versions N and prior, the product receives input or data but does not validate or incorrectly validates that the input has the properties required to process the data safely and correctly, which can induce a denial-of-service condition through a system restart. A vulnerability exists in Patient Information. The vulnerability stems from special elements that may be interpreted as commands when spreadsheet software opens the file. The following products and versions are affected: B.02, C.02, C.03

Show details on source website


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var-201806-0568
Vulnerability from variot

IntelliVue Patient Monitors MP Series (including MP2/X2/MP30/MP50/MP70/NP90/MX700/800) Rev B-M, IntelliVue Patient Monitors MX (MX400-550) Rev J-M and (X3/MX100 for Rev M only), and Avalon Fetal/Maternal Monitors FM20/FM30/FM40/FM50 with software Revisions F.0, G.0 and J.3 have a vulnerability that allows an unauthenticated attacker to access memory ("write-what-where") from an attacker-chosen device address within the same subnet. plural Philips The product contains authentication vulnerabilities.Information is obtained, information is altered, and service operation is disrupted (DoS) There is a possibility of being put into a state. Philips IntelliVuePatientMonitorsMP2 and so on are all products of the Dutch company Philips. The Philips IntelliVuePatientMonitors MP2 is an MP series patient monitor device. The AvalonFetal/MaternalMonitorsFM20 is a maternal and child monitor device. Unauthorized access vulnerabilities exist in several Philips products. An attacker could exploit the vulnerability to access memory from its selected device address (within the same subnet). The following products and versions are affected: Philips IntelliVue Patient Monitors MP2/X2/MP30/MP50/MP70/NP90/MX700/800 Rev. B to Rev. M; IntelliVue Patient Monitors MX400-550 Rev. J to Rev. M; X3/ MX100 M revision; Avalon Fetal/Maternal Monitors FM20/FM30/FM40/FM50 using F.0, G.0 and J.3 software revisions

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var-201806-0571
Vulnerability from variot

IntelliVue Patient Monitors MP Series (including MP2/X2/MP30/MP50/MP70/NP90/MX700/800) Rev B-M, IntelliVue Patient Monitors MX (MX400-550) Rev J-M and (X3/MX100 for Rev M only), and Avalon Fetal/Maternal Monitors FM20/FM30/FM40/FM50 with software Revisions F.0, G.0 and J.3 have a vulnerability that exposes an "echo" service, in which an attacker-sent buffer to an attacker-chosen device address within the same subnet is copied to the stack with no boundary checks, hence resulting in stack overflow. plural Philips The product contains a buffer error vulnerability.Information is obtained, information is altered, and service operation is disrupted (DoS) There is a possibility of being put into a state. Philips IntelliVuePatientMonitorsMP2 and so on are all products of the Dutch company Philips. The Philips IntelliVuePatientMonitors MP2 is an MP series patient monitor device. The AvalonFetal/MaternalMonitorsFM20 is a maternal and child monitor device. A buffer overflow vulnerability exists in PhilipsIntelliVuePatientandAvalonFetalMonitors. An attacker could exploit the vulnerability to read memory from its selected device address (within the same subnet). The following products and versions are affected: Philips IntelliVue Patient Monitors MP2/X2/MP30/MP50/MP70/NP90/MX700/800 Rev. B to Rev. M; IntelliVue Patient Monitors MX400-550 Rev. J to Rev. M; X3/ MX100 M revision; Avalon Fetal/Maternal Monitors FM20/FM30/FM40/FM50 using F.0, G.0 and J.3 software revisions

Show details on source website


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var-201806-0569
Vulnerability from variot

IntelliVue Patient Monitors MP Series (including MP2/X2/MP30/MP50/MP70/NP90/MX700/800) Rev B-M, IntelliVue Patient Monitors MX (MX400-550) Rev J-M and (X3/MX100 for Rev M only), and Avalon Fetal/Maternal Monitors FM20/FM30/FM40/FM50 with software Revisions F.0, G.0 and J.3 have a vulnerability that allows an unauthenticated attacker to read memory from an attacker-chosen device address within the same subnet. plural Philips The product contains an information disclosure vulnerability.Information may be obtained. Philips IntelliVuePatientMonitorsMP2 and so on are all products of the Dutch company Philips. The Philips IntelliVuePatientMonitors MP2 is an MP series patient monitor device. The AvalonFetal/MaternalMonitorsFM20 is a maternal and child monitor device. There is an information disclosure vulnerability in PhilipsIntelliVuePatientandAvalonFetalMonitors. An attacker could exploit the vulnerability to read memory from its selected device address (within the same subnet). The following products and versions are affected: Philips IntelliVue Patient Monitors MP2/X2/MP30/MP50/MP70/NP90/MX700/800 Rev. B to Rev. M; IntelliVue Patient Monitors MX400-550 Rev. J to Rev. M; X3/ MX100 M revision; Avalon Fetal/Maternal Monitors FM20/FM30/FM40/FM50 using F.0, G.0 and J.3 software revisions

Show details on source website


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cve-2020-16228
Vulnerability from cvelistv5
Published
2020-09-11 12:58
Modified
2024-08-04 13:37
Severity ?
Summary
Philips Patient Monitoring Devices Improper Check for Certificate Revocation
Show details on NVD website


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              "lang": "eng",
              "value": "Patient Information Center iX (PICiX) Versions B.02, C.02, C.03, PerformanceBridge Focal Point Version A.01, IntelliVue patient monitors MX100, MX400-MX850, and MP2-MP90 Versions N and prior, IntelliVue X3 and X2 Versions N and prior. The software does not check or incorrectly checks the revocation status of a certificate, which may cause it to use a compromised certificate."
            }
          ]
        },
        "problemtype": {
          "problemtype_data": [
            {
              "description": [
                {
                  "lang": "eng",
                  "value": "IMPROPER CHECK FOR CERTIFICATE REVOCATION CWE-299"
                }
              ]
            }
          ]
        },
        "references": {
          "reference_data": [
            {
              "name": "https://us-cert.cisa.gov/ics/advisories/icsma-20-254-01",
              "refsource": "MISC",
              "url": "https://us-cert.cisa.gov/ics/advisories/icsma-20-254-01"
            }
          ]
        }
      }
    }
  },
  "cveMetadata": {
    "assignerOrgId": "7d14cffa-0d7d-4270-9dc0-52cabd5a23a6",
    "assignerShortName": "icscert",
    "cveId": "CVE-2020-16228",
    "datePublished": "2020-09-11T12:58:13",
    "dateReserved": "2020-07-31T00:00:00",
    "dateUpdated": "2024-08-04T13:37:54.179Z",
    "state": "PUBLISHED"
  },
  "dataType": "CVE_RECORD",
  "dataVersion": "5.1"
}