712012
148
Zoom out
Zoom in
Previous page
1/176
Next page
148
EN
FR
IT
ES
NL
RU
PL
TR
AR
DE
CE-RICHTLINIEN | CE-DIRECTIVES | DIRECTIVES CE | DIRETTIVE CE | DIRECTIVAS CE
EN |
The requirements
of the EU Directive
93/42/EEC in
conjunction with
the EU Directive
2007/47/EC for
class IIa medical
devices were met
according to the
standard
EN 60601-1-2:2007.
CE according to the
EU Directives
2014/35/EU
2014/30/EU,
2011/65/EU,
1907/2006/EC,
2005/69/EC,
93/68/EEC and
2001/95/EC.
The CE marking
for the device
refers to the
EU Directive
93/42/EEC in
conjunction with
the EU Directive
2007/47/EC.
Device classification:
Class IIa.
Furthermore, the
device fulfils the
requirements of the
standards:
IEC 60601-1:2012
EN 60601-1:2006
+A1:2013
IEC 60601-11-
11:2010
EN 66001-1-11:2010
EN 1060-1:1995
+A2:2009
EN 1060-3:1997
+A2:2009
EN 1060-4:2004
D | Die
Anforderungen der
EU-Richtlinie
93/42/EWG in
Verbindung mit
der EU-Richtlinie
2007/47/EG für
Medizinprodukte
der Klasse Ila wurden
gemäß der Norm
EN 60601-1-2:2007
erfüllt.
CE gemäß den
EU-Richtlinien
2014/35/EU,
2014/30/EU,
2011/65/EU,
1907/2006/EG,
2005/69/EG,
93/68/EWG und
2001/95/EG.
Das CE-Zeichen für
das Gerät bezieht
sich auf die
EU-Richtlinie
93/42/EWG in
Verbindung mit
der EU-Richtlinie
2007/47/EG.
Geräteklassifikation:
Klasse IIa.
Des Weiteren erfüllt
das Gerät die
Anforderungen der
Normen:
IEC 60601-1:2012
EN 60601-1:2006
+A1:2013
IEC 60601-11-
11:2010
EN 66001-1-
11:2010
EN 1060-1:1995
+A2:2009
EN 1060-3:1997
+A2:2009
EN 1060-4:2004
ES
| Se ha cumplido con
los requisitos de la
Directiva
europea 93/42/CEE
en conjunción con
la Directiva europea
2007/47/CE para
productos médicos
de la clase IIa en
conformidad con la
norma EN 60601-1-
2:2007.
CE conforme con
las Directivas
europeas
2014/35/UE,
2014/30/UE,
2011/65/UE,
1907/2006/
CE, 2005/69/
CE, 93/68/CEE y
2001/95/CE.
El símbolo CE para
el dispositivo se
refiere a la
Directiva europea
93/42/CEE en
conjunción con la
Directiva europea
2007/47/CE.
Clasificación del
dispositivo: clase IIa.
Por lo demás el
dispositivo cumple
con los requisitos de
las normas:
IEC 60601-1:2012
EN 60601-1:2006
+A1:2013
IEC 60601-11-
11:2010
EN 66001-1-
11:2010
EN 1060-1:1995
+A2:2009
EN 1060-3:1997
+A2:2009
EN 1060-4:2004
IT |
Sono soddisfatti
i requisiti della
Direttiva UE
93/42/CEE in
associazione
alla direttiva UE
2007/47/CE sui
dispositivi medici
della classe Ila, ai
sensi della norma
EN 60601-1-2:2007.
CE ai sensi delle
direttive UE
2014/35/UE,
2014/30/UE,
2011/65/UE,
1907/2006/
CE, 2005/69/
CE, 93/68/CEE e
2001/95/CE.
Il contrassegno CE
sull’apparecchio
si riferisce alla
Direttiva UE
93/42/CEE in
associazione
alla Direttiva UE
2007/47/CE.
Classificazione
dell’apparecchio:
classe IIa.
Inoltre, l’apparecchio
soddisfa i requisiti
delle norme:
IEC 60601-1:2012
EN 60601-1:2006
+A1:2013
IEC 60601-11-
11:2010
EN 66001-1-
11:2010
EN 1060-1:1995
+A2:2009
EN 1060-3:1997
+A2:2009
EN 1060-4:2004
FR |
Les exigences de la
directive
UE 93/42/CEE
en combinaison
avec la directive
UE 2007/47/CE
pour les produits
médicaux de
la classe IIa ont
été remplies
conformément
à la norme
EN 60601-1-2:2007.
CE conformément
aux directives UE
2014/35/UE,
2014/30/UE,
2011/65/UE,
1907/2006/CE,
2005/69/CE,
93/68/CEE et
2001/95/CE.
Le signe CE sur
l’appareil se réfère
à la directive UE
93/42/CEE en
combinaison avec
la directive UE
2007/47/CE.
Classification de
l’appareil: Classe IIa
De plus, l’appareil
satisfait aux exigences
des normes:
IEC 60601-1:2012
EN 60601-1:2006
+A1:2013
IEC 60601-11-
11:2010
EN 66001-1-
11:2010
EN 1060-1:1995
+A2:2009
EN 1060-3:1997
+A2:2009
EN 1060-4:2004
148


Need help? Post your question in this forum.

Forumrules


Report abuse

Libble takes abuse of its services very seriously. We're committed to dealing with such abuse according to the laws in your country of residence. When you submit a report, we'll investigate it and take the appropriate action. We'll get back to you only if we require additional details or have more information to share.

Product:

For example, Anti-Semitic content, racist content, or material that could result in a violent physical act.

For example, a credit card number, a personal identification number, or an unlisted home address. Note that email addresses and full names are not considered private information.

Forumrules

To achieve meaningful questions, we apply the following rules:

Register

Register getting emails for Promed HGP-50 at:


You will receive an email to register for one or both of the options.


Get your user manual by e-mail

Enter your email address to receive the manual of Promed HGP-50 in the language / languages: English, German, Dutch, French, Italian, Polish, Turkish, Spanish as an attachment in your email.

The manual is 1,53 mb in size.

 

You will receive the manual in your email within minutes. If you have not received an email, then probably have entered the wrong email address or your mailbox is too full. In addition, it may be that your ISP may have a maximum size for emails to receive.

The manual is sent by email. Check your email

If you have not received an email with the manual within fifteen minutes, it may be that you have a entered a wrong email address or that your ISP has set a maximum size to receive email that is smaller than the size of the manual.

The email address you have provided is not correct.

Please check the email address and correct it.

Your question is posted on this page

Would you like to receive an email when new answers and questions are posted? Please enter your email address.



Info