Sign In
Upload
Download
Table of Contents
Contents
Add to my manuals
Delete from my manuals
Share
URL of this page:
HTML Link:
Bookmark this page
Add
Manual will be automatically added to "My Manuals"
Print this page
×
Bookmark added
×
Added to my manuals
Manuals
Brands
ProMed Manuals
Blood Pressure Monitor
PBW-5.2
Instruction leaflet
Ce-Richtlinien S; Ce Directives S; Directives Ce S; Direttive Ce S - ProMed PBW-5.2 Instruction Leaflet
Upper arm blood pressure meter
Hide thumbs
1
2
3
4
5
6
7
8
9
10
11
12
13
14
15
16
17
18
19
20
21
22
23
24
25
26
27
28
29
30
31
32
33
34
35
36
37
38
39
40
41
42
43
44
45
46
47
48
49
50
51
52
53
54
55
56
57
58
59
60
61
62
63
64
65
66
67
68
69
70
71
72
73
74
75
76
77
78
79
80
81
82
83
84
85
86
87
88
89
90
91
92
93
94
95
96
97
98
99
100
101
102
103
104
105
106
107
108
109
110
111
112
113
114
115
116
117
118
119
120
121
122
123
124
125
126
127
128
129
130
131
132
133
134
135
136
137
138
139
140
141
142
143
144
145
146
147
148
149
150
151
152
153
154
155
156
157
158
159
160
161
162
163
164
165
166
167
168
169
170
171
172
173
174
175
176
page
of
176
Go
/
176
Contents
Table of Contents
Troubleshooting
Bookmarks
Table of Contents
Advertisement
Available languages
EN
FR
ES
DE
IT
NL
PL
SE
RU
FI
More
Available languages
ENGLISH, page 20
FRANÇAIS, page 36
ESPAÑOL, página 68
DEUTSCH, seite 4
ITALIANO, pagina 52
DUTCH, pagina 84
POLSKI, strona 116
SVENSKA, sida 132
РУССКИЙ, страница 99
SUOMI, sivu 148
CE-R
ICHTLINIEN
Die Anforderungen
der EU-Richtlinie
93/42/EWG in
Verbindung mit
der EU-Richtlinie
2007/47/EG für
Medizinprodukte
der Klasse IIa wurden
gemäß der Norm
EN 60601-1-2:2007
erfüllt.
CE gemäß den
EU-Richtlinien
2006/95/EG,
2004/108/EG
2002/95/EG,
1907/2006/EG,
2005/69/EG,
93/68/EWG und
2001/95/EG.
DE
Das CE-Zeichen
für das Gerät
bezieht sich auf
die EU-Richtlinie
EN
93/42/EWG in
Verbindung mit
der EU-Richtlinie
2007/47/EG.
FR
Geräteklassifikation:
Klasse IIa.
Des Weiteren
IT
erfüllt das Gerät
die Anforderungen
der Normen:
EN 1060-1:1995
ES
+A2:2009
EN 1060-3:1997
+A2:2009
IEC 60601-1:2005
NL
+Corr.1:2006
+Corr.2:2007
EN 60601-1-2:2007
EN 61000-3-2:2006
RU
+A1:2006+A2:2009
EN 61000-3-3:2008
EN 61000-4-2:2009
EN 61000-4-4:2010
PL
EN 61000-4-5:2007
EN 61000-4-6:2009
EN 61000-4-8:2010
EN 61000-4-11:2005
SE
FI
| CE-D
| D
IRECTIVES
The requirements
of the EU directive
93/42/EEC, in
combination with
the EU directive
2007/47/EC for
Class IIa Medical
Products,
have been met in
accordance with the
standard
EN 60601-1-2:2007.
CE in accordance
with the
EU directives
2006/95/EC,
2004/108/EC
2002/95/EC,
1907/2006/EC,
2005/69/EC,
93/68/EEC and
2001/95/EC
The CE mark
for the device
refers to
the EU directive
93/42/EEC in
combination with
the EU directive
2007/47/EC.
Device classification:
Class IIa.
Furthermore, the
device fulfils the
requirements of
the standards:
EN 1060-1:1995
+A2:2009
EN 1060-3:1997
+A2:2009
IEC 60601-1:2005
+Corr.1:2006
+Corr.2:2007
EN 60601-1-2:2007
EN 61000-3-2:2006
+A1:2006+A2:2009
EN 61000-3-3:2008
EN 61000-4-2:2009
EN 61000-4-4:2010
EN 61000-4-5:2007
EN 61000-4-6:2009
EN 61000-4-8:2010
EN 61000-4-11:2005
CE | D
IRECTIVES
I requisiti
Les exigences
della direttiva
de la directive EU
93/42/EEC associée
93/42/EEC in
à la directive EU
relazione con la
2007/47/EC pour les
direttiva 2007/47/EC
produits médicaux
per prodotti medicali
della classe IIa
de classe IIa ont
été respectées
sono stati soddisfatti
conformément à la
ai sensi della norma
norme
EN 60601-1-2:2007.
EN 60601-1-2:2007.
CE ai sensi della
direttive
CE conformément aux
2006/95/EC,
directives EU
2006/95/EC,
2004/108/EC
2004/108/EC
2002/95/EC,
2002/95/EC,
1907/2006/EC,
1907/2006/EC,
2005/69/EC,
93/68/EEC e
2005/69/EC,
93/68/EEC et
2001/95/EC.
2001/95/EC.
La marcatura CE
Le symbole CE
per il dispositivo
se rapporte
si riferisce
alla direttiva
pour l'appareil
93/42/EEC in
à la directive EU
93/42/EEC en
relazione con
association avec
la direttiva
la directive EU
2007/47/EC.
Classificazione di
2007/47/EC.
dispositivi: classe IIa.
Classification de
l'appareil : classe IIa.
Inoltre il dispositivo
En outre,
soddisfa i requisiti
l'appareil est conforme
delle seguenti
norme:
aux exigences
des normes :
EN 1060-1:1995
EN 1060-1:1995
+A2:2009
+A2:2009
EN 1060-3:1997
EN 1060-3:1997
+A2:2009
IEC 60601-1:2005
+A2:2009
+Corr.1:2006
IEC 60601-1:2005
+Corr.1:2006
+Corr.2:2007
+Corr.2:2007
EN 60601-1-2:2007
EN 60601-1-2:2007
EN 61000-3-2:2006
EN 61000-3-2:2006
+A1:2006+A2:2009
EN 61000-3-3:2008
+A1:2006+A2:2009
EN 61000-3-3:2008
EN 61000-4-2:2009
EN 61000-4-2:2009
EN 61000-4-4:2010
EN 61000-4-4:2010
EN 61000-4-5:2007
EN 61000-4-5:2007
EN 61000-4-6:2009
EN 61000-4-8:2010
EN 61000-4-6:2009
EN 61000-4-11:2005
EN 61000-4-8:2010
EN 61000-4-11:2005
168
CE | D
IRETTIVE
IRECTRICES
Se ha cumplido
con los
requisitos de la
Directiva europea
93/42/EEC en
conjunción con la
Directiva europea
2007/47/EC para
productos
médicos de la clase
IIa de acuerdo con
la norma
EN 60601-1-2:2007.
CE conforme con las
Directivas europeas
2006/95/EC,
2004/108/EC,
2002/95/EC,
1907/2006/EC,
2005/69/EC,
93/68/EEC y
2001/95/EC
El símbolo CE
para el dispositivo
se refiere a
la Directiva europea
93/42/EEC en
conjunción con la
Directiva europea
2007/47/EC.
Clasificación del
dispositivo: clase IIa.
Por lo demás
el dispositivo cumple
con los requisitos
de las normas:
EN 1060-1:1995
+A2:2009
EN 1060-3:1997
+A2:2009
IEC 60601-1:2005
+Corr.1:2006
+Corr.2:2007
EN 60601-1-2:2007
EN 61000-3-2:2006
+A1:2006+A2:2009
EN 61000-3-3:2008
EN 61000-4-2:2009
EN 61000-4-4:2010
EN 61000-4-5:2007
EN 61000-4-6:2009
EN 61000-4-8:2010
EN 61000-4-11:2005
CE
Table of
Contents
Previous
Page
Next
Page
1
...
167
168
169
170
Show Quick Links
Quick Links:
Operating the Unit S
Hide quick links:
Permanently
Temporary
Cancel
Advertisement
Chapters
Deutsch
3
English
19
Français
35
Italiano
51
Español
67
Dutch
83
Русский
99
Polski
115
Svenska
131
Suomi
147
Table of Contents
Related Manuals for ProMed PBW-5.2
Blood Pressure Monitor ProMed PBM-3.5 Instruction Leaflet
(156 pages)
Blood Pressure Monitor ProMed HGP-50 Instruction Leaflet
(176 pages)
Blood Pressure Monitor ProMed PBM-4.2 Instruction Leaflet
Upper arm blood pressure meter (172 pages)
Blood Pressure Monitor ProMed BDP-200 Instruction Leaflet
Upper arm blood pressure monitor (176 pages)
Blood Pressure Monitor ProMed 400110 Instruction Manual
Upper arm blood pressure measuring device mtx (184 pages)
Blood Pressure Monitor ProMed BDS-700 Instruction Leaflet
Upper arm blood pressure monitor (180 pages)
Related Content for ProMed PBW-5.2
BDS-700 Ce-Richtlinien
ProMed BDS-700
BDP-200 Ce-Richtlinien S
ProMed BDP-200
PBM-3.5 Ce-Richtlinien S
ProMed PBM-3.5
HGP-50 Ce-Richtlijnen
ProMed HGP-50
Table of Contents
Print
Rename the bookmark
Delete bookmark?
Delete from my manuals?
Login
Sign In
OR
Sign in with Facebook
Sign in with Google
Upload manual
Upload from disk
Upload from URL