343
Equipment Manufacturer
B-K Medical
Mileparken 34
DK-2730 Herlev
Denmark
References
[1] EN 60601–1–1:2001 Medical electrical equipment –Part 1-1: General requirements for
safety. Collateral standard: Safety requirements for medical electrical systems.
[2] EN 60601-1-2:2002 Medical electrical equipment – Part 1-2: General requirements for
safety. Collateral standard: Electromagnetic Compatibility-Requirements and tests.
[3] EN 60601-2-37:2001+A1:2005 Medical electrical equipment – Part 2-37: Particular
requirements for the safety of ultrasonic medical diagnostic and monitoring equipment.
[4] UL 2601-1:2003 Medical Electrical Equipment – Part 1. General Requirements for safety.
[5] CSA C22.2 No. 601.1–M90:2001 Medical Electrical Equipment – Part 1. General Require-
ments for safety.
Approvals
UL International DEMKO (CB certification)
UL Listed
CUL (UL listing for Canada)
TÜV (Germany) - pending
JMI (Japan) - pending
EU Medical Device Directive 93/42/EEC
Market clearance
FDA
Summary of Contents for Pro Focus 2202
Page 1: ...English BB1279 A June 2005 Pro Focus 2202 Extended User Guide ...
Page 14: ...14 ...
Page 15: ...Part 1 Basics ...
Page 16: ......
Page 32: ...32 Chapter 1 ...
Page 48: ...48 Chapter 2 ...
Page 49: ...Part 2 Working with the Image ...
Page 50: ......
Page 98: ...98 Chapter 5 ...
Page 117: ...Part 3 Imaging Modes ...
Page 118: ......
Page 136: ...136 Chapter 8 ...
Page 152: ...152 Chapter 10 ...
Page 164: ...164 Chapter 12 ...
Page 165: ...Part 4 Setting up and Maintaining Your System ...
Page 166: ......
Page 200: ...200 Chapter 13 ...
Page 208: ...208 Chapter 14 ...
Page 209: ...Part 5 Pro Packages ...
Page 210: ......
Page 288: ...288 Chapter 19 ...
Page 313: ...Part 6 Appendixes ...
Page 314: ......
Page 344: ...344 Appendix C ...