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RSL-D-RS-2024B-DCS-EN-1.0-2024-06-12 RayStation 2024B DICOM Conformance Statement.PDF

RAYSTATION 2024B DICOM Conformance Statement Declaration of conformity Complies with Medical Device Regulation (MDR) 2017/745. A copy of the corresponding Declaration of Conformity is available

RSL-D-RC-v2025-IFU-KO-1.0-2025-06-25 RayCare v2025 Instructions for Use.pdf

RAYCARE V2025 사용 지침 Traceback information: Workspace Main version a1007 Checked in 2025-06-25 Skribenta version 5.6.019 적합성 선언문 의료기기규정(MDR) 2017/745를 준수합니다. 해당적합성선언사본은요청시제공됩 니다. 안전 고지

RSL-D-RS-v2025-RN-EL-1.0-2025-04-28 RayStation v2025 Release Notes.pdf

RAYSTATION V2025 Σημειώσεις έκδοσης Traceback information: Workspace Minor updates 1 version a199 Checked in 2025-06-02 Skribenta version 5.6.019 Δήλωση αποποίησης ευθύνης Για πληροφορίες

RSL-D-RP-2024A-DCS-EN-1.0-2023-12-06 RayPlan 2024A DICOM Conformance Statement.pdf

RAYPLAN 2024A DICOM Conformance Statement Declaration of conformity Complies with Medical Device Regulation (MDR) 2017/745. A copy of the corresponding Declaration of Conformity is available on

RSL-D-RP-v2025-DCS-EN-1.0-2025-04-10 RayPlan v2025 DICOM Conformance Statement.pdf

RAYPLAN V2025 DICOM Conformance Statement Disclaimer For information on functionality not available for regulatory reasons, see the Regulatory Information in the RayPlan Instructions for Use.

RSL-D-RP-v2025-RN-CS-2.0-2025-07-04 RayPlan v2025 SP1 Release Notes.pdf

RAYPLAN V2025 SP1 Poznámky k verzi Traceback information: Workspace Main version a1009 Checked in 2025-07-04 Skribenta version 5.6.019 [Disclaimer] Informace o funkcích nedostupných

Website Rayintelligence 2025 V004.webm
RaySearch Annual Report 2023.pdf

RAYSEARCH | 2023 ANNUAL REPORT CONTENTS ABOUT RAYSEARCH .............................................................................. 1 CEO COMMENTS ..........................................

RSL-D-RS-6-IHEROIS-EN-1.0-2019-04-10 RayStation 6 IHE-RO Integration Statement.pdf

RAYSTATION 6 IHE-RO Integration Statement Declaration of conformity Complies with 93/42/EEC Medical Device Directive as amended by M1 to M5. A copy of the

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