99.60 Withdrawal effective Mar 4, 2009
CEN
CEN/TC 215 Respiratory and anaesthetic equipment
European Norm
11.040.10 Anaesthetic, respiratory and reanimation equipment
This part of ISO 10079 specifies safety and performance requirements for manually powered medical suction equipment intended for oro-pharyngeal suction to establish and maintain the patency of the airway. It covers equipment operated by foot or by hand or both (.). Non-electrical suction equipment which may be integrated with electrical equipment is within the scope of this part. This part of ISO 10079 does not apply to electrically powered suction equipment, whether mains electricity or battery-powered, which is dealt with in ISO 10079-1, nor to suction equipment powered from a vacuum or pressure source which is dealt with in ISO 10079-3, nor the following: a) central power supply (by vacuum/compressed air generation), piping systems of vehicles and buildings, and wall connectors; b) catheter tubes, drains, curettes and suction tips; c) syringes; d) dental suction equipment; e) waste gas scavenging systems; f) laboratory suction; g) autotransfusion systems; h) passive urinary drainage; i) closed systems for wound drainage; j) gravity gastric drainage; k) orally operated mucous extractors; l) suction equipment where the collection container is downstream of the vacuum pump; m) equipment marked as suction unit for permanent tracheostomy; n) ventouse (obstetric) equipment; o) neonatal mucous extractors; p) breast pumps; q) liposuction; r) uterine aspiration; s) thoracic drainage.
Legislation related to this standard
WITHDRAWN
EN ISO 10079-2:1996
WITHDRAWN
EN ISO 10079-2:1999
99.60
Withdrawal effective
Mar 4, 2009
WITHDRAWN
EN ISO 10079-2:2009