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About This Item

 

Full Description

This clause of the General Standard applies except as follows:

1.1 Scope

Addition:
This Particular Standard applies to INVASIVE BLOOD PRESSURE MONITORING and measuring EQUIPMENT as defined in 2.101, hereinafter referred to as EQUIPMENT.

This Particular Standard does not apply to catheter tubing, catherter needles, Luer locks, taps and tap tables.

This Particular Standard also does not apply to NON-INVASIVE BLOOD PRESSURE MONITORING EQUIPMENT.

1.2 Object

Replacement:
The object of this Particular Standard is to establish particular requirements for the safety, including the essential performance of EQUIPMENT, as defined in 2.101.

1.3 Particular Standards

Addition:
This Particular Standard refers to IEC 60601-1:1998, Medical electrical equipment - Part 1: General requirements for safety as amended by its amendment 1 (1991) and its amendment 2 (1995).

The General Standard takes into account IEC 60601-1-2:1993, Medical electrical equipment - Part 1: General requirements for safety - 2. Collateral standard: Electromagnetic compatibility - Requirements and tests and IEC 60601-1-4:1996, Medical electrical equipment - Part 1: Collateral Standard Programmable electrical medical systems.

For brevity, IEC 60601 is referred to in this Particular Standard either as the "General Standard"or as the General Requirement(s)".

The numbering of sections clauses or subclauses of this Particular Standard corresponds to that of the General Standard. The changes to the text of the General Standard are specified by the use of the following words: "Replacement" means that the clause or subclause of the General Standard is replaced completely by the text of this Particular Standard.

"Addition" means that the clause or subclause of this Particular Standard is additional to the requirements of the General Standard.

"Amendment" means that the clause or subclause of the General Standard is amended as indicated by the text of this Particular Standard.

Subclauses or figures which are additional to those of the General Standard are numbered starting from 101, additional annexes are lettered AA, BB, etc, and additional items aa), bb), etc.

The term "this Standard"is used to make reference to the General Standard and this Particular Standard taken together.

An asterisk (*) notes clauses for which there is rationale comment in annex AA or annex BB. It is considered that a knowledge of the reasons for these requirements will facilitate the proper application of the standard and be of use in any revision that may be necessitated by changes in clinical practice or as a result of developments in technology.

Where there is no corresponding section, clause or subclause in this Particular Standard, the secion, clause or subclause of the General Standard, although possibly not relevant, applies without modification; where it is intended that any part of the General Standard, although possibly relevant, is not to be applied, a statement to that effect is given in this Particular Standard.

The requirements of this Particular Standard take priority over those of the General Standard and of the Collateral Standards mentioned above.
 

Document History

  1. CAN/CSA C22.2 NO. 60601-2-34:12 (R2022)


    Medical Electrical Equipment - Part 2-34: Particular Requirements for the Safety, Including Essential Performance, of Invasive Blood Pressure Monitoring Equipment (Adopted IEC 60601-2-34:2000, second edition, 2000-10)

    • Most Recent
  2. CAN/CSA C22.2 NO. 60601-2-34-02 (R06)

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    Medical Electrical Equipment - Part 2-34: Particular Requirements for the Safety, Including Essential Performance, of Invasive Blood Pressure Monitoring Equipment (Adopted IEC 60601-2-34:2000, second edition, 2000-10)

    • Historical Version