RFID is used in medical devices to improve authentication, traceability, inventory control, Unique Device Identification (UDI) management and compliance. Despite this, a handful of misconceptions have left manufacturers feeling indecisive around how to use the technology, delaying critical adoption windows and removing what could otherwise be a competitive edge. To clear things up, in this blog we look at five common RFID myths and replace them with facts grounded in real-world applications and data.
Myth 1: RFID Integration Is Too Expensive
Reality: RFID is scalable and often delivers a strong return on investment.
Many manufacturers worry RFID systems require prohibitive upfront costs. But today’s RFID solutions are modular and scalable — you can start small, such as tagging only high-value assets, and expand over time. This phased approach aligns your investment with actual value creation.
RFID helps prevent device loss, streamline processes and simplify regulatory compliance. These benefits often offset the initial cost quickly. Consider the hidden cost of doing nothing: manual tracking errors, product misplacements and slow recall responses can be far more expensive than implementing RFID.
Strategic technological advances have made RFID more affordable and easier to deploy across healthcare facilities. These innovations have in turn broadened RFID adoption by reducing both hardware and integration costs.
In short, RFID is not an expense — it’s an investment that drives operational savings, improves compliance outcomes and increases ROI.
Myth 2: RFID Takes Too Long To Implement
Reality: RFID deployments can be completed in weeks through phased rollouts.
While large IT projects often take months or years, RFID implementation is surprisingly fast and flexible. Many RFID components — tags, readers, middleware and software — are standardized and readily deployable. Manufacturers typically begin with a pilot program targeting a single facility or product line to validate ROI before wider rollout.
For example, this study showed RFID smart cabinets achieving 100% product assignment accuracy in operating rooms within just four to five months. Additionally, hospitals reported transitioning from manual to automated operating room inventory tracking in only 90 days.
These aren’t isolated success stories; they reflect a broader trend. Modern RFID solutions are built to align with existing clinical and operational workflows. Because tags and readers are pre-configured or plug-and-play, and middleware supports out-of-the-box data integration, healthcare facilities and manufacturers alike can roll out functional pilots quickly. Once in place, the benefits — like improved traceability, fewer errors and faster decision-making — become immediately visible, creating momentum for broader adoption.
Implementing RFID doesn’t require reinventing your processes. It’s about layering visibility and automation onto what’s already there. Whether you're tagging surgical kits or finished devices, RFID helps teams track items more efficiently without slowing them down, often going from kickoff to ROI in just a few months.
Myth 3: RFID Integration Is Too Complex for Existing Systems
Reality: RFID is designed to integrate seamlessly with existing infrastructure.
Fear of system complexity is a major barrier. Yet, RFID’s true power comes from its interoperability. Modern RFID systems use open APIs and integration tools to work alongside ERPs, MES platforms, labeling software, clinical databases and warehouse management systems, all without requiring disruptive overhauls. In most cases, RFID doesn’t replace your infrastructure; it enhances it.
Current RFID standards, such as GS1 TDS 2.0 and SGTIN+ EPC encoding, allow manufacturers to encode tags during routine production processes. This compatibility means RFID data can flow directly into backend systems like ERP and EHR platforms, providing real-time insight with minimal configuration. The result is a unified digital thread across the supply chain, enabling traceability from the factory floor to the point of care.
RFID supports phased implementation. You can start by tagging, surgical trays or high-risk components and expand the system gradually — scaling complexities only when you're ready. This flexibility allows organizations to tailor the system to their resources and goals, whether by building in-house capabilities or partnering with experienced system integrators.
RFID also strengthens UDI compliance by automatically capturing and transmitting device identifiers such as lot number, serial number and expiration date, without manual entry. This automation ensures consistent, accurate UDI data through the device's life cycle.
Unlike barcodes and QR codes, which require line-of-sight scanning, RFID can capture multiple items automatically without direct visual alignment. This capability reduces manual entry, speeds up recalls and improves the accuracy of lot numbers, expiration dates and inventory levels. Despite its advanced functionality, RFID adds minimal complexity when tags are integrated with readers, making implementation straightforward. Highly customizable across frequencies, sizes, shapes, form factors and environmental conditions, RFID is versatile enough to support a wide range of medical device applications.
With the right planning, RFID is not just compatible with your systems. It elevates them.
Myth 4: RFID Disrupts Workflows
Reality: RFID enhances workflows by reducing manual labor and errors.
A common fear among medical device manufacturers is that implementing RFID will require a major process overhaul, disrupt existing workflows or burden staff with unfamiliar procedures. In truth, RFID systems are designed to integrate into your current operations, not compete with them. They support automation, accuracy and responsiveness, without altering the foundational processes already in place.
When enhanced with RFID, medical devices can automatically track medication usage and restocking needs in real time. The result is reduced inventory uncertainty, improved compliance and decreased administrative workload, all without adding complexity for staff.
RFID also plays a vital role in safety workflows by enabling a “kill switch” function: tags embedded in medical devices can signal a system to automatically disable or quarantine equipment that’s out of compliance, expired or recalled. This ensures that only safe, approved devices are in circulation — supporting regulatory and patient safety goals and reducing reliance on manual checks.
In asset management, RFID can be used to track the entire life cycle of a device, from production to usage, maintenance and retirement. For high-value items like surgical instruments or electronic equipment, RFID enables automated documentation of cycle counting and autocalibration parameters. Autocalibration routines, for instance, can be tied to RFID data, automatically initiating checks or maintenance alerts when a device hits a usage threshold. This not only saves time but ensures consistent adherence to maintenance protocols and increases patient safety.
RFID tags can be embedded into labels or applied during packaging. Once tagged, items can be tracked automatically through manufacturing, warehousing and distribution without the need for manual scans or handwritten logs. This real-time data stream reduces errors, accelerates handoffs and enhances accountability, which is critical in regulated environments.
Studies have shown that RFID can significantly reduce manual work and eliminate redundant steps. For example, hospitals using RFID to manage anesthesia carts and crash carts reported saving over 17 hours of staff time per week, all without changing the way clinical teams operate. Similarly, RFID-equipped smart cabinets have helped eliminate manual inventory counts and logging, allowing clinical staff to focus on care delivery rather than stock reconciliation.
The evidence is clear: Rather than disrupt workflows, RFID augments them instead.
Myth 5: RFID Doesn’t Work in Medical Environments
Reality: RFID is engineered to withstand medical environment challenges.
A persistent concern is that RFID won’t function reliably in complex medical environments, especially where equipment is metal-heavy, conditions are sterile and interference is common. But in actuality, today’s RFID technology is specifically designed to meet these challenges head-on.
Specialized RFID tags are built to endure the extreme conditions often found in medical device manufacturing, distribution and use. This includes:
- Resistance to multiple sterilization methods, such as GAMMA radiation, VHP/STERRAD gas plasma and steam autoclaves, ensuring that tags remain functional after repeated cleaning cycles
- Temperature resilience, including ambient refrigeration for biologics and cryogenic environments for cell therapies and genetic materials
- Robust durability against moisture, vibration and exposure to harsh chemicals during device handling or reprocessing
Even in facilities where electromagnetic interference (EMI), metal equipment or liquid-filled containers might once have posed problems, modern RFID systems have evolved with enhanced chip designs and improved antenna configurations that continue to operate reliably.
Use cases today span across a wide range of critical workflows, including:
- Monitoring the location and usage of orthopedic implants
- Managing loaner devices to ensure accurate return and refurbishment
- Securing high-value consumables like biologics and injectable therapies
A comprehensive HIMSS report, which reviewed multiple field studies, confirmed RFID’s high reliability in clinical environments. It showed:
- Up to 100% accuracy in real-time patient and staff identification
- Significant reduction in medication administration errors
- 93% accuracy in tracking hand hygiene events, which is key for infection control
- Improved patient safety in ORs, with surgical ID accuracy increasing from 75% to 100%
These aren't theoretical benefits — they’re the result of real-world implementations in environments as rigorous as operating rooms, clean rooms and intensive care units.
RFID has moved beyond proof of concept and into standard practice. It’s a technology engineered for the realities of healthcare, helping providers and manufacturers alike achieve greater safety, accountability and performance without compromise.
Conclusion
RFID has evolved into a proven, flexible solution for medical device manufacturers. It delivers scalable, standards-based technology that improves traceability, compliance and operational efficiency across the product life cycle.
For manufacturers still hesitating, now is the time to look past myths and explore RFID’s real-world benefits. The technology is mature, implementation is straightforward and the potential for measurable improvements is huge.
Ready to explore how RFID can support your medical device operations? Watch our on-demand webinar to learn how manufacturers are unlocking RFID’s full potential.