the International Consortium of Investigative Journalists. Information submitted on conformance with such standards will have a direct bearing on safety and effectiveness determinations made during the review of IDEs, HDEs, PMAs, and PDPs. BROCHURE FDB MedKnowledge, proven in thousands of healthcare contexts, is the industry's most trusted drug database … $5 billion is wasted annually from expired, lost or uncaptured medical device and implantable charge costs. FDB Prizm provides exactly what is needed to empower hospitals, retail pharmacies, payers and EMR system developers to optimally manage DME buying, selling, tracking and recording processes. This database may be searched by a variety of fields and is updated once a week. On January 2, 2019, the price model for database searches changed. This database allows you to search the CDRH's database information on medical devices which may have malfunctioned or caused a death or serious injury during the years 1992 through 1996. This database contains key device identification information submitted to the FDA about medical devices that have Unique Device Identifiers (UDI). This database contains information about current Post-Approval Studies (PAS). Datacenter-3 (New - around first week of August 2019, Now Live - September 4, 2019) An official website of the United States government, : Table 2: Prices for flat fees, valid from 02.01.2019, excluding VAT, office hours: 9am to 12pm and 1 to 4pm(on fridays until 3pm).

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97% increase in recalls. This database contains product names and associated information developed by the Center for all products, both medical and non-medical, which emit radiation. If you have any concerns or issues, please contact NLM Support Center. The Implant Files is an investigation by more than 250 journalists in 36 countries that tracks the global harm caused by medical devices that have been tested inadequately or not at all. IPV4: 3.217.176.226 IPV6: 2607:f220:41f:1140::152 This database contains historical information about CDRH Advisory Committees and Panel meetings through 2008, including summaries and transcripts. Support your members with the right information and provide solutions to reduce cost while improving outcomes. ** Please note that the ABDA database is only accessible to health care professionals within the meaning of § 2 Heilmittelwerbegesetz. This database contains the commercially marketed in vitro test systems categorized as CLIA waived by the FDA since January 31, 2000, and by the Centers for Disease Control and Prevention (CDC) prior to that date. A searchable listing by state and zip code of all mammography facilities certified by the Food and Drug Administration (FDA) as meeting baseline quality standards for equipment, personnel and practices under the Mammography Quality Standards Act of 1992 (MQSA). Learn more about who we are. Learn how FDB supports telemedicine, an increasingly sought-after option for patient and providers.


If your organization uses firewall rules for accessing AccessGUDID, you need to update your firewall rules to allow for these additional IP addresses.

Extensions and additional bookings of flat fees are also possible here. Summaries of safety and effectiveness information is available via the web interface for more recent records. Searchable listing of Humanitarian Device Exemption (HDE) Class III medical devices.

Medical device knowledge is standardized, normalized, and categorized by FDB data experts and structured to power your information system to deliver numerous possibilities to your users. FDB provides drug and medical device databases that helps healthcare professionals make precise decisions.

The FDB Prizm medical device database delivers medical device attributes from a variety of sources, such as FDA, GUDID, manufacturers, industry data pools, and more.
As person reporting or sponsor, you have the option to enter and edit your data in the Medical Devices Information System. IPV4: 165.112.140.152 The status of the action is updated if the FDA identifies a violation and classifies the action as a recall and again when the recall is terminated.

The primary goal for MedSun is to work collaboratively with the clinical community to identify, understand, and solve problems with the use of medical devices.

Detailed Information about the database Medical Devices Addresses (MPADOE, MPADC) Flat fees for database search. The Global Unique Device Identification Database (GUDID) contains key device identification information submitted to the FDA about medical devices that have Unique Device Identifiers (UDI). IPV4: 3.94.60.161

CBER recall information is available here.