Packaging for terminally sterilized medical devices - Sterilization wrap. Requirements and test methods Ingestion-build-224916

Packaging for terminally sterilized medical devices - Sterilization wrap. Requirements and test methods Ingestion-build-2249161 Scope This European Standard specifies test methods and values for materials for sterile barrier systems and or packaging systems that are intended to maintain sterility of terminally sterilized medical devices to the point of use. Other than the general requirements as specified in EN ISO 11607 1 and EN ISO 11607 2 this part of EN 868 specifies materials, test methods and values that are specific to the products covered by this European Standard.

5 Test levels

The methods are not suitable for the determination of insoluble matter in a dyestuff

1) heating water circuit (if installed) does not exceed 6 bar

optical power meter uncertainties

ISO 20145 specifies two methods of measuring the level of acoustic pressure at the outlet of an exhaust silencer:

The document specifies definitions and technical criteria (acceptable sources

and definitions for quantities and units of telebiometrics related to human physiology are given

other than at a high level

component or system without causing damage

BS EN 61158-4-8 provides a highly optimized means of interchanging fixed-length input/output data and variable-length segmented messages between a single master device and a set of slave devices interconnected in a loop (ring) topology

or for use in private information processing systems using Teletex technology

G1 and G2 in foodstuffs for