Web8 jun. 2024 · InterStim (TM) System, Model Numbers: a) TH90G01 b) TH90GFA c) TH90G02 d) TH90G03 Product Usage: The Medtronic Model A510 Clinician application (app) is intended for use with the HH90 Handset and TM90 Communicator to program, adjust, and troubleshoot the Medtronic Models 3023 and 3058 InterStim … Web8 jun. 2024 · InterStim (TM) System, Model Numbers: a) TH90G01 b) TH90GFA c) TH90G02 d) TH90G03 Product Usage: The Medtronic Model A510 Clinician application …
3537 3537 User Manual 1 Medtronic, - FCC ID
Web18 aug. 2024 · Device Recalls Device Safety Communications GUDID Advanced Search; Search Help; Home; About; News ... InterStim™ SureScan™ Version or Model: 978B128 ... Company Name: MEDTRONIC, INC. Primary DI Number: 00763000203726 Issuing Agency: GS1 Commercial Distribution End Date: Device Count: 1 Labeler D-U-N-S® Number *: … WebA correction or removal action taken by a manufacturer to address a problem with a medical device. Recalls occur when a medical device is defective, when it could be a risk to health, or when it is both defective and a risk to health. Learn more about the data here Type of Event Recall Event ID 70271 Event Risk Class Class 2 Event Number chow down leeds location
Medtronic Neuromodulation - InterStim(TM) System - Class 2 …
Web3537 User Manual 1 details for FCC ID LF53537 made by Medtronic, Inc.. Document Includes User Manual User Manual 1. FCC ID.io; Blog; Search; 3537 3537 User Manual … Web23 okt. 2024 · Fridley, Minn.-based Medtronic said in the notice out of Germany that the Medtronic Model 3560030/3560022 percutaneous extension is intended for use with the … Web1 Event Recall of Device Recall Interstim for Urinary Control Manufacturer Medtronic Neuromodulation Manufacturer Address Medtronic Neuromodulation, 800 53rd Ave NE, … genicular nerve block us guided