Persona Medical Certifications

International Regulatory Compliance Information


QUALITY MANAGEMENT SYSTEM

ISO 13485: 2016/ EN ISO 13485: 2016 | VIEW

US FDA Good Manufacturing Practice (GMP)
We are fully compliant 21 CFR Part 820, US FDA Quality Systems Regulations.

QUALITY CERTIFICATIONS AND APPROVALS

EUROPE – CE marking Certificates | VIEW
UNITED STATES – FDA 510(k) cleared/ PMA approved devices | FDA
CERTIFICATE TO FOREIGN GOVERNMENTS | VIEW

GLOBAL REGULATORY REPRESENTATIVES

Shown below are our European representatives for regulatory affairs issues and incident reporting:

Wellkang Ltd
29 Harley Street
LONDON W1G 9QR
England
United Kingdom                                                        Wellkang.Ltd

NOTIFIED BODY / REGISTRAR / CERTIFICATION BODY

Persona Medical Devices maintains ISO and CE certification and is audited every year by our registrar:

SGS North America Inc.
515 West Greens Road
Suite 775
Houston, TX 77067                                                SGS USA


The Food and Drug Administration (FDA or USFDA) is an agency of the United States Department of Health and Human Services and is responsible for regulating and supervising the safety of foods, dietary supplements, drugs, vaccines, biological medical products, blood products, medical devices, radiation-emitting devices, veterinary products, and cosmetics.

The American National Standards Institute or ANSI (pronounced /’ænsi/ AN-see) is a private non-profit organization that oversees the development of voluntary consensus standards for products, services, processes, systems, and personnel in the United States. The organization also coordinates U.S. standards with international standards so that American products can be used worldwide. For example, standards make sure that people who own cameras can find the film they need for that camera anywhere around the globe. ANSI accredits standards that are developed by representatives of standards developing organizations, government agencies, consumer groups, companies, and others. These standards ensure that the characteristics and performance of products are consistent, that people use the same definitions and terms, and that products are tested the same way. ANSI also accredits organizations that carry out product or personnel certification in accordance with requirements defined in international standards.

The International Organization for Standardization (Organisation internationale de normalisation), widely known as ISO (pronounced /’a?so?/), is an international-standard-setting body composed of representatives from various national standards organizations. Founded on 23 February 1947, the organization promulgates worldwide proprietary industrial and commercial standards. It is headquartered in Geneva, Switzerland.[1] While ISO defines itself as a non-governmental organization, its ability to set standards that often become law, either through treaties or national standards, makes it more powerful than most non-governmental organizations. In practice, ISO acts as a consortium with strong links to governments.

The CE marking (also known as CE mark) is a mandatory conformity mark on many products placed on the single market in the European Economic Area (EEA). The CE marking certifies that a product has met EU consumer safety, health or environmental requirements.