Download Inhoudsopgave Inhoud Print deze pagina
Inhoudsopgave

Advertenties

(BZ2100) zijn geldig voor  = 55. Om het nauwkeurigheidspercentage voor
andere hoeken te berekenen, dient u de opgegeven nauwkeurigheid te
vermenigvuldigen met
Als de stromingssnelheid van het bloed de geselecteerde snelheid overstijgt,
treedt aliasing op. Dit wijst op een overbelasting van het meetsysteem.

Literatuur

[1] EN 60529:1991+A1:2000. Specification for degrees of protection provided by enclosures
[2] EN/IEC 60601-1:1990+A1:1993+A2:1995+A13:1996 Medical electrical equipment. Part
[3] EN 60601-2-37:2001+A1:2005+A2:2005 Medical electrical equipment – Part 2-37: Particu-
[4] UL 60601-1:2003 Medical Electrical Equipment - Part 1. General Requirements for Safety.
[5] CSA C22.2 No. 601.1-M90 Medical Electrical Equipment - Part 1. General Requirements
[6] EN 60601-1-2:2001 + A1:2006 Medical electrical equipment - Part 1-2: General require-
[7] EN 60601–1–1:2001 Medical electrical equipment –Part 1-1: General requirements for
[8] Information for Manufacturers Seeking Marketing Clearance of Diagnostic Ultrasound
[9] Acoustic Output Measurement Standard for Diagnostic Ultrasound Equipment.
[10] Standard for Real-Time Display of Thermal and Mechanical Acoustic Output Indices on
[11] Medical Ultrasound Safety. Tweede uitgave. AIUM. 2009.
[12] ALARA Training Program. Ultrasound III Training. BK Medical. 1993.
[13] Bioeffects considerations for the safety of diagnostic ultrasound. Journal of Ultrasound in
44 Hoofdstuk 2
cos
cos
+
1.8
------------------------------------------------
100
cos
(IP code).
1: General requirements for safety.
EN/IEC 60601-1:2006 3rd Ed. Medical electrical equipment. Part 1: General requirements
for basic safety and essential performance.
lar requirements for the safety of ultrasonic medical diagnostic and monitoring equipment.
EN 60601-2-37:2008 Medical electrical equipment – Part 2-37: Particular requirements for
the basic safety and essential performance of ultrasonic medical diagnostic and monitoring
equipment.
for Safety.
ments for safety. Secundaire norm: Elektromagnetische compatibiliteit - Eisen en beproe-
vingen.
EN 60601-1-2:2007 Medical electrical equipment - Part 1-2: General requirements for
basic safety and essential performance. Secundaire norm: Elektromagnetische compatibili-
teit - Eisen en beproevingen.
safety. Secundaire norm: Veiligheidseisen voor medische elektrische systemen.
Systems and Transducers. FDA Center for Devices and Radiological Health. September
2008.
AIUM/NEMA. 2004.
Diagnostic Ultrasound Equipment. AIUM/NEMA. 2004.
Medicine, Vol. 7, Nr. 9 (supplement). September 1988.
Mei 2019
+
0.5
Gebruikershandleiding Flex Focus 1202 (BB1921-O)

Advertenties

Inhoudsopgave
loading

Inhoudsopgave