DANSK DS/ISO 28620 PDF

This International Standard specifies essential requirements and related test methods for non-electrically driven portable infusion devices1). It applies to devices designed for continuous (fixed or adjustable) flow and/or for bolus application. These devices may be used in health care and non-health care settings. They may be applied or administered by health care professionals or by the intended patient. These devices may be pre-filled by the manufacturer or filled before use by a health care professional or the intended patient. This standard does not apply to – electrically driven or electrically controlled infusion pumps that are covered by IEC 60601-2-24; – implantable devices; – enteral feeding pumps; – transdermal delivery devices ; – devices where the energy for infusion is not provided by the device or through active intervention by the patient (e.g. devices only powered by gravity);