PRICES include / exclude VAT
Homepage>BS Standards>11 HEALTH CARE TECHNOLOGY>11.040 Medical equipment>11.040.50 Radiographic equipment>BS EN 60601-2-27:2014 Medical electrical equipment Particular requirements for the basic safety and essential performance of electrocardiographic monitoring equipment
Sponsored link
immediate downloadReleased: 2014-09-30
BS EN 60601-2-27:2014 Medical electrical equipment Particular requirements for the basic safety and essential performance of electrocardiographic monitoring equipment

BS EN 60601-2-27:2014

Medical electrical equipment Particular requirements for the basic safety and essential performance of electrocardiographic monitoring equipment

Format
Availability
Price and currency
English Secure PDF
Immediate download
399.30 EUR
You can read the standard for 1 hour. More information in the category: E-reading
Reading the standard
for 1 hour
39.93 EUR
You can read the standard for 24 hours. More information in the category: E-reading
Reading the standard
for 24 hours
119.79 EUR
English Hardcopy
In stock
399.30 EUR
Standard number:BS EN 60601-2-27:2014
Pages:78
Released:2014-09-30
ISBN:978 0 580 59724 4
Status:Standard
DESCRIPTION

BS EN 60601-2-27:2014


This standard BS EN 60601-2-27:2014 Medical electrical equipment is classified in these ICS categories:
  • 11.040.55 Diagnostic equipment
  • 11.040.50 Radiographic equipment
IEC 60601-2-27:2011 applies to electrocardiographic monitoring equipments used in a hospital environment as well as when used outside the hospital environment, such as in ambulances and air transport. This particular standard also applies to ECG telemetry systems used in a hospital environment. Electrocardiographic monitoring equipments intended for use under extreme or uncontrolled environmental conditions outside the hospital environment, such as in ambulances and air transport, shall comply with this particular standard. Additional standards may apply for those environments of use. This standard is not applicable to electrocardiographic monitors for home use. However, manufacturers should consider using relevant clauses of this standard as appropriate for their intended use. Ambulatory ("Holter") monitors, fetal heart rate monitoring, pulse plethysmographic devices, and other ECG recording equipment are outside the scope of this particular standard. The aim of this third edition is to bring this particular standard up to date with reference to the third edition of the general standard through reformatting and technical changes. The contents of the corrigendum of May 2012 have been included in this copy.