Search Medical Device Listing Number

Search Registration and Listing | FDA

https://www.fda.gov/medical-devices/device-registration-and-listing/search-registration-and-listing

Search the Registration & Listing database ; Establishment Registration and Medical Device Listing Files for Download ; Releasable establishment registration and listing information under the ...

Establishment Registration & Device Listing - Food and …

https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRL/TextSearch.cfm

Establishment Registration & Device Listing - Food and …

https://www.accessdata.fda.gov/scrIpts/cdrh/cfdocs/cfRL/rl.cfm?xss=1

Device Registration and Listing | FDA

https://www.fda.gov/medical-devices/how-study-and-market-your-device/device-registration-and-listing

For assistance with registration and listing status, please contact the CDRH Registration and Listing Help Desk at: Phone: 301-796-7400. Email: …

Medical Device Databases | FDA

https://www.fda.gov/medical-devices/device-advice-comprehensive-regulatory-assistance/medical-device-databases

Apr 6, 2022

AccessGUDID - Identify Your Medical Device

https://accessgudid.nlm.nih.gov/

The Global Unique Device Identification Database (GUDID) contains key device identification information submitted to the FDA about medical devices that have …

How to find the Medical Device Listing Number (MDL Number) …

https://elsmar.com/elsmarqualityforum/threads/how-to-find-the-medical-device-listing-number-mdl-number-from-the-fda-website.45979/

Nov 16, 2017#4. I believe you'd have to contact the manufacturer, per FDA "...medical device listing number (s) are not available publicly. Medical device listing …

How to Register and List | FDA

https://www.fda.gov/medical-devices/device-registration-and-listing/how-register-and-list

Select the DRLM button (Device Registration and Listing Module). Select the "Annual Registration" link from the DRLM main menu. You must select the Annual Registration …

Registration and Listing of Medical Devices during the COVID-19

https://www.fda.gov/medical-devices/coronavirus-covid-19-and-medical-devices/registration-and-listing-medical-devices-during-covid-19-pandemic

Instructions for Annual Registration (PDF-810KB) The facility is required to pay the annual registration user fee using the Device Facility User Fee (DFUF) website …

510(k) Premarket Notification - Food and Drug Administration

https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfPMN/pmn.cfm

510 (k) Premarket Notification. FDA Home. Medical Devices. Databases. A 510 (K) is a premarket submission made to FDA to demonstrate that the device to be marketed is as …