Vieworks Secures CE MDR Approval for Next-Generation X-ray Detector Portfolio
2025-11-21

Vieworks, a global provider of medical and industrial imaging
solutions, announced on the 21st that six of its static X-ray detectors—including
VIVIX-S F series, VIVIX-S 1751S long-format detectors, and the
mid-sized VIVIX-S 4386W—have received CE MDR (Medical Device
Regulation) certification from the European Union.
CE MDR is the mandatory regulatory framework for selling medical
devices in the EU, and its requirements are significantly stricter than those
of the former Medical Devices Directive (MDD).
Vieworks’ detectors met all major criteria, including company-wide
quality management processes and post-market surveillance validity,
demonstrating compliance with the EU’s highest standards for safety and
reliability.
The company’s VIVIX-S F series delivers industry-leading
performance with enhanced resolution, durability and user experience. Featuring
an ultra-fine 99-micrometer pixel pitch, it maximizes clinical image
clarity. The detectors are built with flexible TFT and polyimide substrates,
reducing weight by more than 25% while improving impact resistance.
Software-based scatter correction further strengthens imaging precision for
clinical diagnosis.
Powered by the new certifications, Vieworks expects its mid- to long-term revenue growth to accelerate. The company’s static X-ray detector business surpassed KRW 100 billion in annual sales for the first time last year and recorded a CAGR of 8.9% since 2018.
- Previous
- List

