CVE-2025-69009: Missing Authorization in kamleshyadav Medicalequipment
Missing Authorization vulnerability in kamleshyadav Medicalequipment medicalequipment allows Exploiting Incorrectly Configured Access Control Security Levels.This issue affects Medicalequipment: from n/a through <= 1.0.9.
AI Analysis
Technical Summary
CVE-2025-69009 identifies a missing authorization vulnerability in the kamleshyadav Medicalequipment product, affecting versions up to 1.0.9. The core issue stems from incorrectly configured access control security levels, allowing unauthenticated remote attackers to perform actions that should require authorization. The vulnerability does not impact confidentiality or availability but compromises the integrity of the system, meaning attackers could potentially alter data or device behavior without detection. The CVSS 3.1 vector (AV:N/AC:L/PR:N/UI:N/S:U/C:N/I:L/A:N) indicates network attack vector, low attack complexity, no privileges or user interaction needed, and unchanged scope. No patches or known exploits exist yet, but the lack of authorization checks in a medical device context is concerning due to the critical nature of healthcare data and device operation. The vulnerability could be exploited to manipulate medical equipment settings or data, potentially endangering patient care or violating compliance requirements. The absence of CWE identifiers limits detailed classification, but the issue clearly relates to access control misconfigurations. The vendor and product are relatively niche, but the impact on healthcare environments is significant given the sensitive nature of medical equipment. The vulnerability was published at the end of 2025, indicating a recent discovery.
Potential Impact
For European organizations, especially healthcare providers and hospitals using kamleshyadav Medicalequipment, this vulnerability poses a risk to the integrity of medical device operations and data. Unauthorized modifications could lead to incorrect medical readings, treatment errors, or falsified patient data, undermining patient safety and trust. Regulatory frameworks such as GDPR and the EU Medical Device Regulation (MDR) impose strict requirements on data integrity and device security, so exploitation could result in legal and financial consequences. The medium severity rating reflects that confidentiality and availability are not directly impacted, but the integrity compromise alone is critical in a medical context. Additionally, the lack of authentication requirements and remote exploitability increase the threat surface. European healthcare networks, often interconnected and under constant cyber threat, could be targeted by attackers aiming to disrupt medical services or conduct espionage. The absence of known exploits provides a window for mitigation, but also means defenders must act proactively.
Mitigation Recommendations
1. Immediately audit and strengthen access control configurations on all kamleshyadav Medicalequipment devices to ensure proper authorization enforcement. 2. Implement network segmentation to isolate medical equipment from general IT networks, limiting exposure to untrusted sources. 3. Employ strict firewall rules and intrusion detection/prevention systems to monitor and block unauthorized access attempts targeting these devices. 4. Conduct regular security assessments and penetration testing focused on access control mechanisms of medical devices. 5. Engage with the vendor for timely patches or firmware updates addressing the vulnerability; if unavailable, consider compensating controls such as disabling remote management features. 6. Train healthcare IT staff on recognizing signs of device tampering or anomalous behavior. 7. Maintain comprehensive logging and monitoring of device access and configuration changes to enable rapid incident response. 8. Review and update incident response plans to include scenarios involving medical device integrity breaches. 9. Collaborate with national cybersecurity agencies and healthcare regulators to share threat intelligence and best practices.
Affected Countries
Germany, France, United Kingdom, Italy, Spain, Netherlands, Sweden, Belgium
CVE-2025-69009: Missing Authorization in kamleshyadav Medicalequipment
Description
Missing Authorization vulnerability in kamleshyadav Medicalequipment medicalequipment allows Exploiting Incorrectly Configured Access Control Security Levels.This issue affects Medicalequipment: from n/a through <= 1.0.9.
AI-Powered Analysis
Technical Analysis
CVE-2025-69009 identifies a missing authorization vulnerability in the kamleshyadav Medicalequipment product, affecting versions up to 1.0.9. The core issue stems from incorrectly configured access control security levels, allowing unauthenticated remote attackers to perform actions that should require authorization. The vulnerability does not impact confidentiality or availability but compromises the integrity of the system, meaning attackers could potentially alter data or device behavior without detection. The CVSS 3.1 vector (AV:N/AC:L/PR:N/UI:N/S:U/C:N/I:L/A:N) indicates network attack vector, low attack complexity, no privileges or user interaction needed, and unchanged scope. No patches or known exploits exist yet, but the lack of authorization checks in a medical device context is concerning due to the critical nature of healthcare data and device operation. The vulnerability could be exploited to manipulate medical equipment settings or data, potentially endangering patient care or violating compliance requirements. The absence of CWE identifiers limits detailed classification, but the issue clearly relates to access control misconfigurations. The vendor and product are relatively niche, but the impact on healthcare environments is significant given the sensitive nature of medical equipment. The vulnerability was published at the end of 2025, indicating a recent discovery.
Potential Impact
For European organizations, especially healthcare providers and hospitals using kamleshyadav Medicalequipment, this vulnerability poses a risk to the integrity of medical device operations and data. Unauthorized modifications could lead to incorrect medical readings, treatment errors, or falsified patient data, undermining patient safety and trust. Regulatory frameworks such as GDPR and the EU Medical Device Regulation (MDR) impose strict requirements on data integrity and device security, so exploitation could result in legal and financial consequences. The medium severity rating reflects that confidentiality and availability are not directly impacted, but the integrity compromise alone is critical in a medical context. Additionally, the lack of authentication requirements and remote exploitability increase the threat surface. European healthcare networks, often interconnected and under constant cyber threat, could be targeted by attackers aiming to disrupt medical services or conduct espionage. The absence of known exploits provides a window for mitigation, but also means defenders must act proactively.
Mitigation Recommendations
1. Immediately audit and strengthen access control configurations on all kamleshyadav Medicalequipment devices to ensure proper authorization enforcement. 2. Implement network segmentation to isolate medical equipment from general IT networks, limiting exposure to untrusted sources. 3. Employ strict firewall rules and intrusion detection/prevention systems to monitor and block unauthorized access attempts targeting these devices. 4. Conduct regular security assessments and penetration testing focused on access control mechanisms of medical devices. 5. Engage with the vendor for timely patches or firmware updates addressing the vulnerability; if unavailable, consider compensating controls such as disabling remote management features. 6. Train healthcare IT staff on recognizing signs of device tampering or anomalous behavior. 7. Maintain comprehensive logging and monitoring of device access and configuration changes to enable rapid incident response. 8. Review and update incident response plans to include scenarios involving medical device integrity breaches. 9. Collaborate with national cybersecurity agencies and healthcare regulators to share threat intelligence and best practices.
Affected Countries
Technical Details
- Data Version
- 5.2
- Assigner Short Name
- Patchstack
- Date Reserved
- 2025-12-29T11:18:21.372Z
- Cvss Version
- 3.1
- State
- PUBLISHED
Threat ID: 695450addb813ff03e2bec08
Added to database: 12/30/2025, 10:22:37 PM
Last enriched: 1/21/2026, 1:52:49 AM
Last updated: 2/7/2026, 10:41:09 AM
Views: 28
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