Proceq USA Inc. PQLIVE Manuale Utente
5
Schwerzenbach, 31.08.2017
Patrick Waller
Head of Supply Chain
Head of Supply Chain
Schwerzenbach, 31.08.2017
Patrick Waller
Head of Supply Chain
Head of Supply Chain
SWISS MADE
Swiss made Declaration
Product:
Proceq GPR Live
Models:
Basic / Pro / Unlimited
Proceq Part Number:
393 10 x00
We confirm that the Proceq GPR Live instrument was developed and
manufactured in Switzerland and fulfills the requirements needed for the
declaration “Made in Switzerland” or “Swiss Made.”
manufactured in Switzerland and fulfills the requirements needed for the
declaration “Made in Switzerland” or “Swiss Made.”
The requirements for industrial products are in detail specified in the National
Swiss Trademark Protection Statute (Art.47-50, MSchG) covering goods and
services.
Swiss Trademark Protection Statute (Art.47-50, MSchG) covering goods and
services.
Declaration of Conformity
Product:
Proceq GPR Live
Models:
Basic / Pro / Unlimited
Proceq Part Number:
393 10 x00
Manufacturer:
Proceq SA
Address:
Ringstrasse 2, 8603 Schwerzenbach,
Switzerland
We confirm that the Proceq GPR Live instrument conforms with the following
directives and standards:
Health:
directives and standards:
Health:
EN 62479:2010
Safety standards:
EN 61010-1:2010
Laser classification:
EN 60825-1:2014
IP classification:
IP 54
Battery directive:
2006/66/EC
Restriction of hazardous
substances (RoHS):
substances (RoHS):
2011/65/EC
Radio equipment directive:
2014/53/EU(RED)
Draft ETSI EN 301 489-1 v. 2.2.0
Draft ETSI EN 301 489-33 v 2.2.0
EN 61326-1:2013
Radio compatibility:
ETSI EN 302 066 v 2.1.1
The conformity is based on all essential and specific radio test suites for that
radio equipment category identified by the involved Notified Body. The noti-
fied body IMQ S.p.A. (identification number 0051) performed the EU-type ex-
amination in compliance with Annex III Module B of the 2014/53/EU Directive
and issued the EU-type examination Certificate No. 0051-RED-0043.
This device complies with Part 15 of the FCC Rules and RSS-220 of IC. Opera-
tion is subject to the following two conditions: (1) this device may not cause
harmful interference, and (2) this device must accept any interference re-
ceived, including interference that may cause undesired operation. Changes
or modifications not expressly approved by the party responsible for compli-
ance could void the user’s authority to operate the equipment.
radio equipment category identified by the involved Notified Body. The noti-
fied body IMQ S.p.A. (identification number 0051) performed the EU-type ex-
amination in compliance with Annex III Module B of the 2014/53/EU Directive
and issued the EU-type examination Certificate No. 0051-RED-0043.
This device complies with Part 15 of the FCC Rules and RSS-220 of IC. Opera-
tion is subject to the following two conditions: (1) this device may not cause
harmful interference, and (2) this device must accept any interference re-
ceived, including interference that may cause undesired operation. Changes
or modifications not expressly approved by the party responsible for compli-
ance could void the user’s authority to operate the equipment.
English
FCC ID: 2ANPE-PQLIVE
IC: xxxxx-PQLIVE