Art. 2200S
 
Multifunction Tub

Multisteril



Tecno-Gaz S.p.A. has been able to create a new and revolutionary device that can automatically carry out all the major preparation phases for th e sterilization cycle, such as disinfection, cleansing, rinsing, drying, without human intervention, without any professional risk and with a reduction in the overall time taken.
A device that is unique in the world and indispensable for every facility that carries out sterilization.



Assistants’ expenditure of time
Assistants spend a lot of time for the preparation phase to tools sterilization, because of multiple and complex manual procedures.
Multisteril does not require human presence.

Risk factor
The manipulation of tools and potential infectious materials is a very important factor and it must be kept under strict control, both for operators’ protection and the responsibility of the owner of the studio.
Multisteril cancels the risk.

Management protocol
There is the sterilization if the procedure of preparation of materials is done properly, if not, the whole process is completely nullified.
Multisteril performs correctly all the cycles.

Spaces
Space is another important problem, in fact, sterilization rooms often have small size and rationalization of space assumes a considerable value.
Multisteril can do all the process filling 40 cm.

Overall costs
Cost is an important component which must be brought under control.
With Multisteril every cycle costs about 2 Euros.

 

Structure








Standbye



 

Phases of the Process






 

Certification

  
 


 

Technical Data

  





 

 
Technical features
Power supply voltage 230±10% Vac
Maximum current of fuses 6 A
Power supply voltage frequency 50 Hz
Maximum electric power absorbed 1000 W
Net weight of product 20 Kg
Product width 415,00
Product height 415,00
Product depth 530,00
HIBC Code +E3092200S4H
Risk class of medical device Classe I
GMDN Code 36749
CND Code Z12011302
Registration number at Italian Ministry of Health 304613
Starting year of manufacturing and marketing 2010
TECNO-GAZ product type code VM
Direttiva 93/42/CEE del Consiglio, del 14 giugno 1993, concernente i dispositivi medici.
Council Directive 93/42/EEC of 14 June 1993 concerning medical devices.
Directive 93/42/CEE du Conseil, du 14 juin 1993, relative aux dispositifs médicaux.
Richtlinie 93/42/EWG des Rates vom 14. Juni 1993 über Medizinprodukte.
Directiva 93/42/CEE del Consejo, de 14 de junio de 1993, relativa a los productos sanitarios.
Direttiva 2006/95/CE del Parlamento europeo e del Consiglio, del 12 dicembre 2006 , concernente il ravvicinamento delle legislazioni degli Stati membri relative al materiale elettrico destinato ad essere adoperato entro taluni limiti di tensione
Directive 2006/95/EC of the European Parliament and of the Council of 12 December 2006 on the harmonisation of the laws of Member States relating to electrical equipment designed for use within certain voltage limits
Directive 2006/95/CE du Parlement européen et du Conseil du 12 décembre 2006 concernant le rapprochement des législations des États membres relatives au matériel électrique destiné à être employé dans certaines limites de tension
Richtlinie 2006/95/EG des Europäischen Parlaments und des Rates vom 12. Dezember 2006 zur Angleichung der Rechtsvorschriften der Mitgliedstaaten betreffend elektrische Betriebsmittel zur Verwendung innerhalb bestimmter Spannungsgrenzen
Directiva 2006/95/CE del Parlamento Europeo y del Consejo, de 12 de diciembre de 2006 , relativa a la aproximación de las legislaciones de los Estados miembros sobre el material eléctrico destinado a utilizarse con determinados límites de tensión
Direttiva 2004/108/CE del Parlamento europeo e del Consiglio, del 15 dicembre 2004, concernente il ravvicinamento delle legislazioni degli Stati membri relative alla compatibilità elettromagnetica e che abroga la direttiva 89/336/CEE.
Directive 2004/108/EC of the European Parliament and of the Council of 15 December 2004 on the approximation of the laws of the Member States relating to electromagnetic compatibility and repealing Directive 89/336/EEC.
Directive 2004/108/CE du Parlement européen et du Conseil du 15 décembre 2004 relative au rapprochement des législations des États membres concernant la compatibilité électromagnétique et abrogeant la directive 89/336/CEE.
Richtlinie 2004/108/EG des Europäischen Parlaments und des Rates vom 15. Dezember 2004 zur Angleichung der Rechtsvorschriften der Mitgliedstaaten über die elektromagnetische Verträglichkeit und zur Aufhebung der Richtlinie 89/336/EWG.
Directiva 2004/108/CE del Parlamento Europeo y del Consejo, de 15 de diciembre de 2004, relativa a la aproximación de las legislaciones de los Estados miembros en materia de compatibilidad electromagnética y por la que se deroga la Directiva 89/336/CEE.
Classificazione del dispositivo medico ai sensi della direttiva 93/42/CEE (Allegato IX) - Classification of medical devices pursuant to Directive 93/42/EEC (Annex IX) - Classification du dispositif médical conformément à la directive 93/42/CEE (Annexe IX) - Klassifizierung des medizinischen Geräts gemäß der EWG-Richtlinie 93/42 (Anlage IX) - Clasificación del dispositivo médico en virtud de la Directiva 93/42/CEE (Anexo IX).
Durata: Temporanea - Period: Temporary - Durée: Temporaires - Daurer: Vorübergehende - Duración: Temporales
Dispositivo non invasivo - Not Invasive Devices - Dispositifs non invasifs - Un Invasive Vorrichtungen - Dispositivos no invasivos
Dispositivo medico attivo - Active medical device - Dispositif médical actif - Aktive medizinische Vorrichtung - Dispositivo médico activo
Classe I (secondo la Regola 2-11) - class I (in accordance with Rule 2-11) - classe I (conformément à la règle 2-11) - Klasse I (gemäß Regel 2-11) - clase I (según la Regla 2-11)
CEI EN 61326-1:2007
CEI EN61010:2001
 
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