AccessGUDID - Identify Your Medical Device

Web Name: AccessGUDID - Identify Your Medical Device

WebSite: http://accessgudid.nlm.nih.gov

ID:155503

Keywords:

Identify,AccessGUDID,Your,

Description:

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). The FDA is establishing the unique device identification system to adequately identify devices sold in the U.S.- from manufacturing through distribution to patient use. You can use AccessGUDID to search for specific medical devices or download all the GUDID data at once. AccessGUDID also offers RSS feeds and APIs to connect you directly to the data. Update 8/2/2019 - AccessGUDID beta is live, please visit https://accessgudid-beta.nlm.nih.gov/ Update 8/29/2019 - AccessGUDID beta will be promoted to production on September 4, 2019. Update 9/4/2019 - AccessGUDID beta now in production, please visit https://accessgudid.nlm.nih.gov/ We will be adding two new data centers with new IP addresses for AccessGUDID. We expect these data centers to be operational in beta mode around the first week of August 2019 and in production mode around the first week of September 2019. If your organization uses firewall rules for accessing AccessGUDID, you need to update your firewall rules to allow for these additional IP addresses. If you have any concerns or issues, please contact NLM Support Center. Datacenter-1 (Current - since 2015) IPV4: 130.14.16.152 IPV6: 2607:f220:41e:1016::152 Datacenter-2 (Current - since 2015) IPV4: 165.112.140.152 IPV6: 2607:f220:41f:1140::152 Datacenter-3 (New - around first week of August 2019, Now Live - September 4, 2019) IPV4: 3.94.60.161 IPV4: 3.217.176.226 Datacenter-4 (New - around first week of August 2019, Now Live - September 4, 2019) IPV4: 52.36.232.238 IPV4: 54.203.164.238 Download the latest full releases and update files provided to the NLM by the FDA.

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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).

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