Spasciani RN Instrucciones De Uso página 21

conformity assessment procedure: Italcert S.r.l., Viale Sarca 336, 20126 Milan – Italy, n° 0426.
6.4. ATEX
All the models, excluded RN BIBO and RN FR BIBO, can be provided in the ATEX version.
The devices are approved with a voluntary Test Certificate (Annex 3 of the 2014/34/UE Directive) issued by:
Albarubens S.r.l, Via G. Ferrari 21/N – 21047 Saronno (VA) – Italia, O.N. n°2632.
7. MARKING
All the important parts related to the safety of the device are marked with the serial number and production date.
1. On the reducer, there is an adhesive label with a bar code (13 digits) and 9-digit, permanently printed number,
whose seven last numbers correspond to the bar code present on the label. The reducer is sealed in the factory and
the last inspection date is printed on it. The serial number of the device is a unique number for each self-contained
breathing apparatus.
2. On the demand valve, there is an adhesive label with a bar code (13 digits). In addition to the bar code, a 9-digit
number is printed on the demand valve and the seven last digits correspond to the bar code assigned.
3. All the hoses are marked with the production date.
4. The membrane of the demand valve and other rubber parts has a "clock" dater reporting the year and month of
manufacture.
5. The entire device has a label on a metal plate affixed to the belt (see label example) and which contains all the
markings required by the Directives and Technical standards of reference:
- Manufacturer name and address (A)
- Type of device (SCBA) (G) and model name (B)
- Marking (E) that indicates the essential requirements respectively established by Regulation 2016/425/EU and
Directive 2014/68/UE were met, followed by the number of the Notified Body that performed the production control
(N° 0426 Italcert S.r.l., V.le Sarca, 336, 20126 Milan - Italy)
- wheel mark (D) (only for MED type) indicating that they meet the essential requirements laid down by Directive
2014/90/UE followed by the number of the Notified Body that carries out the control of production (N° 0426 Italcert
S.r.l., V.le Sarca, 336, 20126 Milan - Italy) and the year of its affixing.
- Reference standard as per Regulation (EU) 2016/425: EN 137:2006 and classification (Type 1 or Type 2) (C);
- Reference standard as per 2014/90/UE Directive: ISO 23269-2:2011 (H)
- Maximum operating pressure (PS) and minimum and maximum temperature of operation (TS) (F)
- Year and month of manufacture and next date of servicing (I)
- Expiration date of approval Mod.B MED (L).
8. ATEX SELF-CONTAINED BREATHING APPARATUSES
All the indications contained in a box with the Ex logo shown on the side refer to explosion risk and
indicate those assemblies produced by SPASCIANI S.p.A. suitable to work in the presence of potentially
Example of a label
USE IN POTENTIALLY EXPLOSIVE ENVIRONMENTS
CAUTION
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