IEC 60601-3-1:1996
IEC 60601-3-1:1996
| Title | Medical electrical equipment - Part 3-1: Essential performance requirement for transcutaneous oxygen and carbon dioxide partial pressure monitoring equipment |
| Abstract | Specifies essential requirements for the performance of transcutaneous oxygen and carbon dioxide partial pressure monitoring equipment. Applies to transcutaneous monitors intended for use with adults, children and neonates, and includes the use of these devices in foetal monitoring during birth. Does not apply to haemoglobin saturation oximeters or to devices applied to surfaces of the body other than the skin such as conjunctiva or mucosa. |
| Issue Date | 1996-08-07 |
| Category | MED |
| Included in IECEE System | 2007-10-01 |
| Purchase | webstore |
| Test Report Form | No information declared |
| Testing Equipment List | No information declared |
DISCLAIMER: National differences
The National differences and Group differences, National Deviations and Special National conditions (SNC), are based solely on information provided to the Secretariat by the IECEE Member Bodies and/or NCBs and other sources. The IEC/IECEE is not responsible for, nor will it take any position related to, the accuracy or validity of the information provided. To verify the current status of this type of information, we recommend contacting the Member Body (MB) or National Certification Body (NCB) of the relevant country.
Group Differences are applicable for CENELEC member countries: Austria, Belgium, Bulgaria, Croatia, Cyprus, the Czech Republic, Denmark, Estonia, Finland, France, Germany, Greece, Hungary, Iceland, Ireland, Italy, Latvia, Lithuania, Luxembourg, Malta, the Netherlands, Norway, Poland, Portugal, Republic of North Macedonia, Romania, Serbia, Slovakia, Slovenia, Spain, Sweden, Switzerland, Turkey and the United Kingdom.
No information declared
No information declared
No information declared
Id | Name | City | Country |
|---|---|---|---|
13359 | Gyeonggi-do | Korea, Republic of |