Explore medical devices and equipment — how they work, how they’re made, and the technologies behind their design and use.
Examine bioethical dilemmas, regulatory gaps, and legal concerns in 3D bioprinting of human tissues and organs including cell sourcing, transplantability, and future frameworks.
Explore frequent failure modes, reliability issues, and proven manufacturing strategies to improve microfluidic device performance in medical and diagnostic fields.
See how ISO 10993-1:2025 changes biocompatibility strategy for device makers. Get practical details on updated risk assessment, testing, legacy device impact, and regulatory hurdles.
Analysis of recent ISO 11135 and ISO 10993-7 changes, with focus on new validation and residue requirements, hurdles for device manufacturers, and practical impact.
Troubleshoot medical grade polycarbonate issues in device manufacturing. Address bubbles, cracking, fogging, assembly fit, and impurity compliance with actionable solutions.
A technical guide to using Polyether Ether Ketone (PEEK) in medical devices, covering key advantages, limitations, failure modes, biocompatibility, and processing challenges.
A detailed, actionable guide for surgeons and surgical teams addressing technical failures, common malfunctions, and troubleshooting practices for endoscopic staplers.
A practical analysis of additive manufacturing challenges for medical devices: quality, reproducibility, material validation, regulation, skills, and post-processing.
A practical troubleshooting guide for operating room staff and biomeds to solve common Electrosurgical Unit (ESU) issues like power loss, sparking, and safety concerns.
Identify common ultrasonic welding problems in medical device manufacturing—like weak welds, flash, and cosmetic issues—and apply proven troubleshooting steps.