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Cybersecurity

SBOMs for Medical Devices: Why HTM Teams Need Them

An SBOM lists the software components inside a device. Why that list matters, what it should contain and how to use it when a vulnerability is announced.

26 October 2026Continue reading ▶
Cybersecurity

Patching Legacy Medical Devices That No Longer Update

Some medical devices stopped receiving updates entirely. Why the patch may not exist, and which compensating controls are defensible when it does not.

26 October 2026Continue reading ▶
Regulations and Standards

Unique Device Identification in Hospital Device Records

A UDI ties inventory, service history and recall notices to one object. What the code contains, who assigns it, and where hospital records usually break down.

26 October 2026Continue reading ▶
Sterilization

Low-Temperature Sterilization: Steam Alternatives Compared

Steam destroys some devices outright. How the main low-temperature processes differ, where their material limits sit, and why the instructions for use govern.

26 October 2026Continue reading ▶
Sterilization

Sterile Processing Competency: Assessing Real Skill

A training file is not evidence of skill. What to observe in sterile processing, how to test inspection and release decisions, and how to record the result.

26 October 2026Continue reading ▶
Medical Device Industry

Right to Repair in Medical Device Service Contracts

Ownership often stops at the enclosure. Where service barriers sit, how manufacturers defend them, and which contract terms preserve access years later.

26 October 2026Continue reading ▶
Editorial note. This article is general education, not a procedure and not professional advice. Before you change anything in your own setting, check the current standard, the manufacturer instructions and your organisation's policy, and involve the people responsible for clinical safety. This site carries no outbound promotional links.