Hettich ROTO SILENTA 630 RS Mode D'emploi page 67

Rating plate
3.2 European registration
Device conformity
Single Registration Number
AB5005en
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Fig. 1: Rating plate
1 Item number
2 Serial number
3 Revision
4 Equipment number
5 Data matrix code
6 any labelling indicating whether medical device or in vitro diagnostic
medical device
7 Global Trade Item Number (GTIN)
8 Date of manufacture
9 Serial number
10 any EAC mark, CE mark
11 Country of manufacture
12 Date of manufacture
13 Mains frequency
14 Maximum kinetic energy
15 Maximum permissible density
16 Manufacturer's address
17 any Coolant circuit pressure
18 any Coolant capacity
19 any Coolant type
20 Revs per minute
21 Performance values
22 Mains voltage
23 any Device designation
24 Manufacturer's logo
Device conformity according to EU directives.
Notified body:
mdc medical device certification GmbH – Notified Body CE 0483
Tel: +49 (0)711 253597 0
Fax: +49 (0)711 258597 10
E-mail: mdc@mdc-ce.de
Website: www.mdc-ce.de
Address: Kriegerstrasse 6, D-70191 Stuttgart, Germany
SRN: DE-MF-000010680
Rev.: 20 / 01.2024
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Device overview
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