IEC 60601-2-50:2000/COR1:2001
(Corrigendum)Corrigendum 1 - Medical electrical equipment - Part 2-50: Particular requirements for the safety of infant phototherapy equipment
Corrigendum 1 - Medical electrical equipment - Part 2-50: Particular requirements for the safety of infant phototherapy equipment
General Information
- Status
- Published
- Publication Date
- 28-Mar-2001
- Technical Committee
- SC 62D - Particular medical equipment, software, and systems
- Current Stage
- DELPUB - Deleted Publication
- Start Date
- 24-Mar-2009
- Completion Date
- 13-Feb-2026
Relations
- Effective Date
- 05-Sep-2023
- Effective Date
- 05-Sep-2023
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Frequently Asked Questions
IEC 60601-2-50:2000/COR1:2001 is a standard published by the International Electrotechnical Commission (IEC). Its full title is "Corrigendum 1 - Medical electrical equipment - Part 2-50: Particular requirements for the safety of infant phototherapy equipment". This standard covers: Corrigendum 1 - Medical electrical equipment - Part 2-50: Particular requirements for the safety of infant phototherapy equipment
Corrigendum 1 - Medical electrical equipment - Part 2-50: Particular requirements for the safety of infant phototherapy equipment
IEC 60601-2-50:2000/COR1:2001 is classified under the following ICS (International Classification for Standards) categories: 11.040.60 - Therapy equipment. The ICS classification helps identify the subject area and facilitates finding related standards.
IEC 60601-2-50:2000/COR1:2001 has the following relationships with other standards: It is inter standard links to IEC 60601-2-50:2000, IEC 60601-2-50:2009. Understanding these relationships helps ensure you are using the most current and applicable version of the standard.
IEC 60601-2-50:2000/COR1:2001 is available in PDF format for immediate download after purchase. The document can be added to your cart and obtained through the secure checkout process. Digital delivery ensures instant access to the complete standard document.
Standards Content (Sample)
IEC 60601-2-50(E)
(First edition – 2000)
Medical electrical equipment –
Part 2-50: Particular requirements for the safety
of infant phototherapy equipment
CORRIGENDUM 1
Page 15
*34 Ultraviolet radiation
Replace the existing text by the following new text:
This clause of the General Standard applies, except as follows:
Replacement:
Effective ultraviolet irradiance shall not exceed
–5 -4
for 180 nm < λ ≤ 400 nm ≤1,0 × 10 mW/cm² (1,0 × 10 W/m²)
at any point of the EFFECTIVE SURFACE AREA.
Compliance with this requirement is checked by testing.
Page 22
Annex AA
(informative)
Guidance and rationale for particular subclauses
Addition to Item 34, page 23:
See also IRPA Guidelines on protection against non-ionizing radiation, edited by A.S.
Duchéne et al. Pergamon Press: Chapter 3: Guidelines on limits of exposure to ultraviolet
radiation of wavelengths between 180 nm and 400 nm (incoherent optical radiation), pages
42-52.
March 2001
In this publication the exposure limits (EL) were given for the near-ultraviolet UV-A spectral
region (315 nm – 400 nm). The total radiant exposure incident on the unprotected skin should
not exceed the values given in table AA.1.
Values for the relative spectral effectiveness, S , are given up to 400 nm to expand the action
λ
spectrum into the UV-A for determining the EL for skin exposure.
To determine the effective irradiance of a broadband source weighted against the peak of the
spectral effectiveness curve (270 nm), the following weighting formula should be used:
E = ∑ E × S × Δ
eff λ λ λ
where:
E = effective irradiance in W/m² normalized to a monochromatic source at 270 nm
eff
E = spectral irradiance from measurements in W/m²
λ
S = relative spectral effectiveness (unitless)
λ
Δ
= bandwidth in nanometers of the calculation or measurement intervals
λ
These ELs should be used as guides in the control of expo
...




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