UNI 11341 : 2010
Current
The latest, up-to-date edition.
BUBBLING HUMIDIFIERS FOR MEDICAL USE - FUNDAMENTAL REQUIREMENTS
04-02-2010
INTRODUZIONE
1 SCOPO E CAMPO DI APPLICAZIONE
2 RIFERIMENTI NORMATIVI
3 TERMINI E DEFINIZIONI
4 COMPONENTI DI UN TIPICO SISTEMA DI UMIDIFICAZIONE
5 REQUISITI GENERALI
6 METODI DI PROVA
7 MARCATURA, COLORI E IMBALLAGGIO
8 INFORMAZIONI FORNITE DAL FABBRICANTE
APPENDICE A (informativa) - RAZIONALE
BIBLIOGRAFIA
This standard is applicable to bubbling humidifiers for medical use intended to rise water content in medical gases for patient.
Committee |
CT 44
|
DocumentType |
Standard
|
PublisherName |
Ente Nazionale Italiano di Unificazione (UNI)
|
Status |
Current
|
UNI CEI EN 980 : 2009 | SYMBOLS FOR USE IN THE LABELLING OF MEDICAL DEVICES |
UNI EN ISO 10524-1 : 2006 | PRESSURE REGULATORS FOR USE WITH MEDICAL GASES - PART 1: PRESSURE REGULATORS AND PRESSURE REGULATORS WITH FLOW-METERING DEVICES |
UNI EN ISO 15001 : 2012 | ANAESTHETIC AND RESPIRATORY EQUIPMENT - COMPATIBILITY WITH OXYGEN |
UNI EN ISO 8185 : 2009 | RESPIRATORY TRACT HUMIDIFIERS FOR MEDICAL USE - PARTICULAR REQUIREMENTS FOR RESPIRATORY HUMIDIFICATION SYSTEMS |
UNI EN 13544-2 : 2009 | RESPIRATORY THERAPY EQUIPMENT - PART 2: TUBING AND CONNECTORS |
ISO 32:1977 | Gas cylinders for medical use — Marking for identification of content |
UNI EN ISO 7396-1 : 2013 | MEDICAL GAS PIPELINE SYSTEMS - PART 1: PIPELINE SYSTEMS FOR COMPRESSED MEDICAL GASES AND VACUUM |
UNI EN ISO 10524-3 : 2013 | PRESSURE REGULATORS FOR USE WITH MEDICAL GASES - PART 3: PRESSURE REGULATORS INTEGRATED WITH CYLINDER VALVES |
UNI EN ISO 4135 : 2002 | ANAESTHETIC AND RESPIRATORY EQUIPMENT - VOCABULARY |
UNI EN ISO 19054 : 2006 | RAIL SYSTEMS FOR SUPPORTING MEDICAL EQUIPMENT |
UNI EN ISO 5359 : 2015 | ANAESTHETIC AND RESPIRATORY EQUIPMENT - LOW-PRESSURE HOSE ASSEMBLIES FOR USE WITH MEDICAL GASES |
UNI EN ISO 15002 : 2008 | FLOW-METERING DEVICES FOR CONNECTION TO TERMINAL UNITS OF MEDICAL GAS PIPELINE SYSTEMS |
UNI CEI EN ISO 14971 : 2012 | MEDICAL DEVICES - APPLICATION OF RISK MANAGEMENT TO MEDICAL DEVICES |
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