The Medical Device Safety Act

The development stage is one of the most significant steps in the entire manufacturing process. During this stage, engineers and designers can work out any errors, inconsistencies, or failures in the machine before full development.

When manufacturing a medical device for patient safety, development is a priority. Because of this, the U.S. Food and Drug Administration (FDA) has set forth standards regarding medical device use and safety.

These standards should make it easier for manufacturers to build prototypes that adhere to medical safety to ensure these devices act as intended.

The Medical Device Safety Act was introduced in the U.S. in 1990.

Enacted to enhance public protection and patient safety, the act states that the FDA must be notified when any medical product causes illness, injury, or death to an individual. Broadly, it’s a type of medical device patient safety act intended to limit the negative impacts of poor device manufacturing.

Upon such notification, the FDA takes action to track or possibly enact device recalls for these products. Because of this act, hospitals and other health care facilities are required by law to report to the FDA any manufacturer of any medical devices not adhering to device safety and effectiveness testing.

In this way, organizations can do their part to maintain healthcare device safety through Medical Device Act adherence.

What is Considered a Medical Device?

Per section 201 (h) of the Food, Drug, and Cosmetic Act, a medical device is “an instrument, apparatus, implement, machine, contrivance, implant, in vitro reagent, or other similar or related article, including a component part, or accessory.” which is recognized in the official National Formulary, or the United States Pharmacopoeia, or any supplement to them.”

The category includes everything from a gauze pad to the disinfectant used to sterilize an electronic medical device, like a monitor or keypad.

How Does the Medical Device Safety Act Affect the Prototyping Process?

The answer is, at the beginning. The FDA has five specific steps in the medical device safety development process:

  1. Device Discovery and Concept
  2. Preclinical Research-Prototype
  3. Pathway to Approval
  4. FDA Review
  5. FDA Post-Market Safety Monitoring

We will focus on the first two steps and their relevance to medical device use and safety.

Medical Device Discovery

The Federal Food, Drug, and Cosmetic Act, section 513, established a risk-based device classification system for medical devices. The various devices are classified differently during this initial stage of the process.

  • General controls or Class I devices are the least risky for public health and include surgical tools, oxygen masks, etc.
  • Class II devices pose more risk to the patient and therefore are subject to both general and special controls including specific performance standards and medical device safety testing.
  • Class III devices involve the support or sustaining of life and are often implanted in the body, presenting a much more substantial risk to the patient. Because of this, Class III devices are subject to all ‘controls’ as well as pre-approval.

The manufacturers of these devices must prove the safety and effectiveness of the device. Therefore, Class II and Class III devices must adhere to stricter safety standards in the prototyping process.

medical device for patient safety

Preclinical Research Prototype  

Once a concept for a device is classified, manufacturers know what types of controls, pre-approvals, testing services, and safety standards they will need for full FDA approval.

From there they begin to build a prototype (not for human use!) utilizing ALL of these standards. These prototypes are each produced in controlled, laboratory settings. At this stage, again, using medical device safety standards and testing, manufacturers continually refine the prototype thereby learning more about its potential use in the health care industry.

Failure by manufacturers to adhere to the safety standards can delay the production process and possibly hinder public health best practices.

Your Trustworthy Medical Device Partner

RBC’s engineers ensure your project follows all medical device safety standards.

Developing a Production-Ready Medical Device Prototype

The professional manufacturer incorporates device testing services and safety standards during every phase of the prototyping process, ensuring a positive development timeline.

If a manufacturer dismisses specific medical device safety testing, a device may fail its usability testing and require reconfiguration and additional device testing.

In addition to the safety standards for the devices mentioned above, the medical safety device act requires that manufacturers maintain compliance with additional regulations including:

  • IEC 62366
  • IEC 60601
  • IEC 60601-1
  • IEC 60601-1-2
  • IEC 60601-1-6
  • ISO 13485
  • ISO 9001
  • ISO 14971
  • FDA

When a manufacturer successfully develops a prototype that complies with safety standards and proves effective, they can approach the FDA to market the device.

The Importance of Safety Standards in the Prototyping Process

With over 250,000 deaths reported annually, medical device safety and standards have become more crucial than ever. Fortunately, safety and the Medical Device Act work in tandem with each other.

The global market of medical devices is large and complicated. RBC Medical Innovations specializes in helping medical device companies navigate this market and bring their products to the healthcare industry faster and with fewer delays.

Contact us today to learn how we can help you with your challenges in medical device manufacturing.

Share This Post

More To Explore

MDR vs MDD
Uncategorized

What You Need to Know About EU MDR

Modern medical products are an undoubtable miracle, but they didn’t achieve the safety or effectiveness we see today without some stringent and strategic frameworks in