Medical electrical equipment - Part 2: Particular requirements for the safety of automatic cycling indirect blood pressure monitoring equipment

Specifies particular requirements for the safety of automatic cycling indirect blood pressure monitoring equipment, with special attention being paid to the avoidance of hazards due to the inflation process.

Medizinische elektrische Geräte - Teil 2: Besondere Festlegungen für die Sicherheit von automatischen zyklischen indirekten Blutdrucküberwachungsgeräten

Appareils électromédicaux - Partie 2: Règles particulières de sécurité des appareils de surveillance de la pression sanguine prélevée indirectement, automatiquement et périodiquement

Spécifie les prescriptions particulières relatives à la sécurité des appareils de surveillance de la pression sanguine prélevée indirectement, automatiquement et périodiquement, une attention spéciale étant apportée aux mesures à prendre pour éviter les risques dus à l'opération de gonflement.

Medical electrical equipment - Part 2: Particular requirements for the safety of automatic cycling indirect blood pressure monitoring equipment (IEC 60601-2-30:1995)

General Information

Status
Withdrawn
Publication Date
17-Jul-1995
Withdrawal Date
31-Mar-1996
Drafting Committee
IEC/SC 62D - IEC_SC_62D
Parallel Committee
IEC/SC 62D - IEC_SC_62D
Current Stage
9960 - Withdrawal effective - Withdrawal
Start Date
01-Feb-2003
Completion Date
01-Feb-2003

Relations

Effective Date
29-Jan-2023

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Frequently Asked Questions

EN 60601-2-30:1995 is a standard published by CLC. Its full title is "Medical electrical equipment - Part 2: Particular requirements for the safety of automatic cycling indirect blood pressure monitoring equipment". This standard covers: Specifies particular requirements for the safety of automatic cycling indirect blood pressure monitoring equipment, with special attention being paid to the avoidance of hazards due to the inflation process.

Specifies particular requirements for the safety of automatic cycling indirect blood pressure monitoring equipment, with special attention being paid to the avoidance of hazards due to the inflation process.

EN 60601-2-30:1995 is classified under the following ICS (International Classification for Standards) categories: 11.040.50 - Radiographic equipment. The ICS classification helps identify the subject area and facilitates finding related standards.

EN 60601-2-30:1995 has the following relationships with other standards: It is inter standard links to EN 60601-2-30:2000. Understanding these relationships helps ensure you are using the most current and applicable version of the standard.

EN 60601-2-30:1995 is associated with the following European legislation: EU Directives/Regulations: 93/42/EEC; Standardization Mandates: M/023. When a standard is cited in the Official Journal of the European Union, products manufactured in conformity with it benefit from a presumption of conformity with the essential requirements of the corresponding EU directive or regulation.

EN 60601-2-30:1995 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)


SLOVENSKI STANDARD
01-september-1998
Medical electrical equipment - Part 2: Particular requirements for the safety of
automatic cycling indirect blood pressure monitoring equipment (IEC 60601-2-
30:1995)
Medical electrical equipment -- Part 2: Particular requirements for the safety of automatic
cycling indirect blood pressure monitoring equipment
Medizinische elektrische Geräte -- Teil 2: Besondere Festlegungen für die Sicherheit von
automatischen zyklischen indirekten Blutdrucküberwachungsgeräten
Appareils électromédicaux -- Partie 2: Règles particulières de sécurité des appareils de
surveillance de la pression sanguine prélevée indirectement, automatiquement et
périodiquement
Ta slovenski standard je istoveten z: EN 60601-2-30:1995
ICS:
11.040.50 Radiografska oprema Radiographic equipment
2003-01.Slovenski inštitut za standardizacijo. Razmnoževanje celote ali delov tega standarda ni dovoljeno.
...

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