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DRC scraps device registration tax after negative feedback

The Democratic Republic of Congo is scrapping its widely criticised device registration tax (Registre des Appareils Mobiles / RAM) from 1st March.

DRC scraps device registration tax after negative feedback

The Democratic Republic of Congo is scrapping its widely criticised device registration tax (Registre des Appareils Mobiles / RAM) from 1st March.

Updates on EU EUDAMED UDI, Device Registration and other Global Health Authorities, Upcoming Webinar Hosted by Xtalks

Updates on EU EUDAMED UDI, Device Registration and other Global Health Authorities, Upcoming Webinar Hosted by Xtalks Share Article In this free webinar, the featured speakers will discuss preparation for EUDAMED UDI submissions and what you need to know for EUDAMED device registration. They will provide an update on other global health authorities and how Reed Tech can help with your UDI submissions and device registrations. Register for this webinar and bring your specific questions concerning UDI, medical device registration scenarios, data elements and requirements. TORONTO (PRWEB) May 04, 2021 This webinar will give an update concerning Unique Device Identifier (UDI) preparation focused on EU EUDAMED UDI and device registration, plus any newly-posted guidance and data dictionary information concerning the six EUDAMED modules. Additionally, the speakers will report on global health authorities including Sout

InnerScope Hearing Technologies (OTC: INND) Completes FDA Class II Medical Device Registration for its Hearing Aid Devices

Share this article Share this article ROSEVILLE, Calif., March 3, 2021 /PRNewswire/  InnerScope Hearing Technologies Inc. (OTC: INND) ( InnerScope ) announced today it has completed and updated the FDA Medical Device Registration for Class II Hearing Aid, Air Conduction with Wireless Technology ( FDA Medical Device Registration ). The completion of the FDA Medical Device Registration (Registration Establishment Number 3014545266) for InnerScope s Nexus HD, HearIQ ITC, HearIQ4, and the HearIQ20, its newest family of rechargeable hearing aid devices, and as well as its Alpha Series of hearing aid devices. The FDA Medical Device Registration is one of the last steps needed for InnerScope to launch its latest in Direct-to-Consumer Hearing Aid Technology with its Smartphone App-Controlled Self-Fitting – Self-Adjusting Rechargeable Hearing Aids with built-in Professional Remote Programming & Support Service ( Self-Fitting Hearing Aids ).

Innerscope Hearing Technologies, Inc : InnerScope Hearing Technologies (INND) Completes FDA Class II Medical Device Registration for its Hearing Aid Devices

Innerscope Hearing Technologies, Inc : InnerScope Hearing Technologies (INND) Completes FDA Class II Medical Device Registration for its Hearing Aid Devices
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