Signifier Medical Technologies Secures European Union Medical Device Regulation (EU MDR) Certification for eXciteOSA®

Contributed by: Business Wire

Logo

Tags

Managed Care

Health Technology

Health

Medical Devices

eXciteOSA

More Like This

Signifier Medical Technologies Announces Milestone Order of 10,000 eXciteOSA Devices by Leading Home Medical Equipment Provider, Spectrum Sleep Solutions Inc.

CMS Sets Pricing with New HCPCS Codes for eXciteOSA Therapy, Expanding Access to Innovative Daytime Sleep Apnea Treatment

Signifier Medical Technologies Announces Upcoming Publication of Randomized Controlled Trial Results Examining High-Intensity (Active) Vs. Low-Intensity (Sham) Neuromuscular Electrical Stimulation in Patients for 6 Weeks

Signifier Medical Technologies Announces Publication of a New Study Exploring Cost-Effectiveness of Neuromuscular Electrical Stimulation for the Treatment of Mild Obstructive Sleep Apnea

Inspire Medical Systems, Inc. Announces CE Mark Certification under the European Union’s Medical Device Regulation for Inspire Therapy

Inspire Medical Systems, Inc. Announces CE Mark Certification of Full-Body MRI Compatibility under the European Union’s Medical Device Regulation

Inspire Medical Systems, Inc. Announces Countrywide Reimbursement in France

PR Newswire associated0

Neoss® Group receives EU Medical Device Regulation (MDR) certifications for implants and abutments