STIMPOD 410-450 Swedish.indd - Xavant Technology

IEC 60601-2-28:2017 - SIS

4-SWE (2020-03). Läs mer om produkten: We improve freedom SS-EN IEC 60601 [2] och det medicintekniska produktdirektivet (MDD [8]) kan påverka drifts- förutsättningarna. Avvikelser från standardlösningar måste kunna han IEC 60601-2-52:2009. Medical electrical equipment - Part 2-52: particular requirements for the basic safety and essential performance of 2010 Welch Allyn SM4033SE Rev A. Säkerhetsstandarder. • IEC 60601-1/A2: 1995. • IEC 60601-1-4/A1: 1999. • IEC 62366: 2007.

Iec 60601-2

Drifttemperatur: 0 °C till 50 ° detta gör att garantin inte längre gäller. STIMPOD (NMS400) har följande standard: • IEC 60601-1, IEC 60601-2-10. • IEC 60601-1-2: CISPR 11 Grupp1 klass B; IEC/TR 62348 (Gratis) Mapping between the clauses of the third edition of IEC SS-EN 60601-2-13 ”Anestesistandarden” – Elektrisk utrustning för medicinskt Särskilda fordringar på simulatorer för strålterapi IEC 60601-2-29:1999 EN 60601-2-29:1995 +A1:1996 Anmärkning 2.1 Datum passerat (1.4.2002). En sängram med integrerade grindar och delbara gavlar som är säker och enkel att använda. Testad och godkänd enligt IEC 60601-2-52. Funktion; Produktfakta Standarden är en internationell standard, IEC 60601-1-2, som antagits som europeisk standard och nu fastställts som svensk standard av SEK Uppfyller tillämpliga krav i UL 2601, AAMI DF80,.

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The IEC shall not be held responsible for identifying any or all such patent rights. International Standard IEC 60601-2-33 has been prepared by subcommittee 62B: Diagnostic imaging equipment, of IEC technical committee 62: Electrical equipment in medical practice.

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International Standard IEC 60601-2-2 has been prepared by subcommittee 62D: Electromedical equipment, of IEC technical committee 62: Electrical equipment in medical practice. This third edition of IEC 60601-2-2 cancels and replaces the second edition published in 1991, International Standard IEC 60601-2-33 has been prepared by subcommittee 62B: Diagnostic imaging equipment, of IEC technical committee 62: Electrical equipment in medical practice.

Fastställelsedatum: 1969-12-31.
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I AED-läget tillåter enheten en defibrillering endast om rådgivningssystemet ger rådet att defibrillera. IEC 60601-2-2:2017 applies to the basic safety and essential performance of HF surgical equipment and HF surgical accessories. HF surgical equipment having a rated output power not exceeding 50 W (for example for micro-coagulation, or for use in dentistry or ophthalmology) is exempt from certain of the requirements of this particular standard.

AED:n är skyddad mot vattenstänk i enlighet med IEC 60529. Klassificerad av ETL Semko IEC 60601-2-4, Sektion 36.202.3 (20 V/m). AAMI DF39, Sektion Sängen har elektriskt ställbart chockläge/hjärtläge. Princess Vega är en svensktillverkad säng som är godkänd enligt standarden IEC 60601-2-52:2009 och EMC- ed alla relevanta standarder: IEC 60601-2, ISO 10535.
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strålterapi - Deutsch-Übersetzung – Linguee Wörterbuch

IEC: 60601-2-4 Edition 3.1 2018-02 CONSOLIDATED VERSION : Medical electrical equipment - Part 2-4: Particular requirements for the basic safety and essential performance of cardiac defibrillators: 01/30/2014: General Plastic Surgery/ General Hospital: 6-321: IEC: 60601-2-52 Edition 1.0 2009-12 • Replaced IEC 60601-2-38 and EN 1970 bed standards • Key elements of the new standard are: 4. Specification of safe working load and patient weight 5. Ensuring stability and electrical safety By purchasing a bed that conforms to the new IEC/ EN 60601-2-52 bed standard, you can ensure your bed stocks provide essential safety for your IEC 60601-2-25 Ed. 2.0 b:2011 Medical electrical equipment - Part 2-25: Particular requirements for the basic safety and essential performance of electrocardiographs "IEC 60601-2-25:2011 applies to the basic safety and essential performance of electrocardiographs intended by themselves or as a part of a medical electrical system, for the production of electrocardiogram reports for diagnostic Therefore IEC 60601-2-7 and IEC 60601-2-32 are not part of the IEC 60601-1 3rd edition scheme for DENTAL EXTRA-ORAL X-RAY EQUIPMENT.

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The standard has of course been updated to fit with IEC 60601-1:2005 (the 3rd edition). Also, similar to IEC 60601-2-27, the opportunity has been taken to International standard IEC 60601-2-52 has been prepared by IEC subcommittee 62D: Electromedical equipment, of IEC technical committee 62: Electrical equipment in medical practice, and by ISO technical committee 173: Assistive products for persons with disability. IEC 60601-2-52:2009 applies to the basic safety and essential performance of medical beds intended for adults.

60601-2-44 Amend. 1 IEC:2002(E) – 3 – dz N T D (z) CTDI = + ∫ × − 50 mm 50 mm 100 where D(z) is the DOSE PROFILE along a line z perpendicular to the TOMOGRAPHIC PLANE, where dose is reported as ABSORBED DOSE to air; N is the number of TOMOGRAPHIC SECTIONS produced in a single axial scan of the X-RAY SOURCE; T is the NOMINAL TOMOGRAPHIC SECTION THICKNESS. IEC 60601-2-41 First edition 2000-02 Medical electrical equipment – Part 2-41: Particular requirements for the safety of surgical luminaires and luminaires for diagnosis Appareils électromédicaux – Partie 2-41: Règles particulières de sécurité pour les éclairages chirurgicaux et les éclairages de diagnostic Reference number IEC 30 rows 2018-09-21 IEC 60601-2-52:2009 applies to the basic safety and essential performance of medical beds intended for adults.