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PAVmed Receives European CE Mark Certification for its


PAVmed Receives European CE Mark Certification for its CarpX® Minimally Invasive Carpal Tunnel Device
May 25, 2021 09:30 ET
| Source:
PAVmed Inc.
PAVmed Inc.
NEW YORK, May 25, 2021 (GLOBE NEWSWIRE)
PAVmed Inc. (Nasdaq: PAVM, PAVMZ) (the “Company” or “PAVmed”), a highly differentiated, multi-product, commercial-stage medical device company, today announced that it has received CE Mark certification for its CarpX
® minimally invasive carpal tunnel device.
EU-based Notified Body TÜV Rhineland LGA Products GMBH issued a CE Certificate, effective May 24, 2021, declaring that CarpX conforms to the essential requirements of Medical Device Directive 93/42/EEC. With CE Mark secured, CarpX may now be marketed in CE Mark European countries, which include the European Economic Area (the EU, Norway, Iceland and Lichtenstein), Switzerland, and, until July 1, 2023, the United Kingdom. ....

United Kingdom , Jim Heins Katie Gallagher , Shaun Oneil , Mark Carp , Matt Ennis , Lishan Aklog , Mike Havrilla , Its Gi Health , Lucid Diagnostics Inc , Drug Administration , Exchange Commission , Pavmed Inc , Globe Newswire Pavmed Inc , Medical Device Directive , European Economic Area , Chief Executive , Esophageal Cell Collection , Esophageal Ablation Device , Its Minimally Invasive Interventions , Minimally Invasive Device , Carpal Tunnel , Infusion Therapy , Implantable Intraosseous Vascular Access Device , Intravenous Infusion Set , Emerging Innovations , Seriesw Warrants ,

SciBase receives important European MDR certification


SciBase receives important European MDR certification
STOCKHOLM, May 10, 2021 /PRNewswire/
SciBase Holding AB ( SciBase ) [STO:SCIB], a leading developer of augmented intelligence-based solutions for skin disorders, announced today that it has been granted certification under the new Medical Device Regulation (MDR).
MDR is a set of mandatory legal requirements central for all companies selling medical devices in the EU. The new regulation comes into effect on May 26
th. SciBase is one of very few medical device manufacturers to have completed the MDR certification, after an intensive two year process. With the MDR Certification in place SciBase can release new products, indications and functionality such as their new Non-melanoma Skin cancer (NMSC) application. ....

United States , Simon Grant , Scibase Holding , European Union , Prnewswire Scibase Holding Ab , Medical Device Regulation , Non Melanoma Skin , Medical Device Directive , Non Melanoma Skin Cancer , Electrical Impedance Spectroscopy , Artificial Intelligence , Base Holding , First North Growth Market , ஒன்றுபட்டது மாநிலங்களில் , சிமோன் மானியம் , ஐரோப்பிய தொழிற்சங்கம் , மருத்துவ சாதனம் ஒழுங்குமுறை , அல்லாத மெலனோமா தோல் , மருத்துவ சாதனம் உத்தரவு , அல்லாத மெலனோமா தோல் புற்றுநோய் , மின் மின்மறுப்பு ஸ்பெக்ட்ரோஸ்கோபி , செயற்கை உளவுத்துறை , அடித்தளம் வைத்திருத்தல் , முதல் வடக்கு வளர்ச்சி சந்தை ,