Mar-Med is an ISO 13485 certified company

FDA Logo | FDA Guidelines | Food and Drug Administration | Mar-Med | Emergency Medicine | Medical Devices
FDA Quality System Regulation

Mar-Med is an American company and is therefore registered with the FDA and regulated under the FDA’s QSR system. The quality systems for FDA-regulated products (food, drugs, biologics, and devices) are known as current good manufacturing practices (CGMP’s). These CGMP requirements for devices in part 820 (21 CFR part 820) were authorized by the Federal Food, Drug, and Cosmetic Act (the act). Mar-Med diligently maintains compliance with these regulations in order to ensure the high quality of our products.

More information: Read FDA QSR regulations

ISO 13485:2016

ISO 13485 is the international standard that specifies requirements for a quality management system where an organization needs to demonstrate its ability to provide medical devices and related services that consistently meet customer requirements and regulatory requirements applicable to medical devices and related services. The primary objective of ISO 13485 is to facilitate harmonized medical device regulatory requirements for quality management systems. Mar-Med is ISO 13485 certified, ensuring the quality of our products.

More information: Read ISO 13485

National Standards Authority of Ireland | NSAI Guidelines | Quality of Standards | Mar-Med Business Standards | Emergency Medicine | Medical Devices | Mar-Med
Notified Body – NSAI

The National Standards Authority of Ireland (NSAI) serves as our notified body. In that role, they serve as that guarantor that we maintain a quality system in compliance with ISO 13485. Chris Morrell, Vice President of the NSAI notes that, “By having ISO 13485 certification, those who use the Tourni-Cot product can have peace of mind in the quality of Mar-Med’s manufacturing and continuous improvement processes. We at NSAI hope that this certification opens up new markets for their Tourni-Cot product.”

More information: Read NSAI’s Website

CE Mark | CE Approved Products | Emergency Medical Devices CE Marked | CE Marked Products by Mar-Med | Medical Devices | Mar-Med
CE Marked

Mar-Med products carry a CE mark, which means that we are compliant with the EU’s Medical Device Directives. Any medical device placed on the European market must meet ‘harmonized standards’ to have a presumption of conformity to the Directives. The core legal framework consists of three directives:

More information: Read Conformity Assessment and the CE Mark, How the United Kingdom Avoids Finger Amputations

Sample Request
Call Now Button