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  BFI’s $50M innovation full stack to accelerate India’s medtech ecosystem,   April 10, 2026
  BD delivers next-generation TIPS innovation to advance portal hypertension care across the European Union,   April 09, 2026
  Artivion announces Endospan’s NEXUS Aortic Arch System receives US FDA approval,   April 08, 2026
  InVera Medical receives US FDA 510(k) clearance for InVera Infusion Device, a novel non-thermal catheter for enhanced infusion of sclerosant for CVD,   April 08, 2026
  UK and US deepen regulatory cooperation on medical devices, building on wider pharmaceutical partnership,   April 06, 2026
  Chugai Pharma files regulatory application with Japanese MHLW for medical device component of the Port Delivery Platform with ranibizumab,   March 20, 2026
  India’s Rs. 1,000 crore MedTech Fund signals strategic shift toward domestic manufacturing,   March 17, 2026
  Abbott introduces more flexible, easier to guide through the heart’s arteries drug eluting stent XIENCE Skypoint in India,   March 11, 2026
  Singapore sets global first by reaching WHO’s highest classification for medical device regulation,   March 11, 2026
  BD’s Revello Vascular Covered Stent receives CE marking to treat atherosclerotic lesions in common and external iliac arteries,   March 09, 2026
  UK MHRA launches a consultation on indefinite recognition of CE-marked medical devices,   February 18, 2026
  InVera Medical’s new vein infusion device receives European CE Mark approval,   February 16, 2026
  Affera momentum continues as Medtronic announces CE Mark in Europe & US IDE first cases for Sphere-360 PFA catheter to treat paroxysmal atrial fibrillation,   January 27, 2026
  Onward Medical completes two additional BCI implants paired with spinal cord stimulation technology to restore thought-driven movement,   January 23, 2026
  Abbott receives CE Mark for TactiFlex Duo Ablation Catheter to treat patients with abnormal heart rhythms,   January 22, 2026
  US FDA approves updated label for Miach Orthopaedics’ BEAR implant to include significantly lower risk of osteoarthritis,   January 16, 2026
  MTaI seeks Centre to align medtech customs and GST structures with other priority sectors,   January 06, 2026
  Establishment Labs Holdings submits Motiva implants to US FDA for approval in primary and revision breast reconstruction,   December 31, 2025
  US FDA grants 510(k) clearance to StimLabs’ Theracor, a first human umbilical cord-derived medical device sheet,   December 31, 2025
  US FDA approves Edwards Lifesciences' SAPIEN M3 mitral valve replacement system, a first transseptal transcatheter therapy to treat mitral regurgitation,   December 26, 2025

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