Manufacturer information
Batch code / Lot number
Catalogue number / Reference number
(01)1569431111XXXX(11)YYMMDD
(21)WWWWWWWWW
(01)1569431111XXXX(11)YYMMDD
(10)ZZZZZZ
Unique Device Identifier (UDI); the Application Identifier
(01) represents the device identifier (DI)
(“1569431111XXXX”), the Application Identifier (11) the
production date/date of manufacture (“YYMMDD”, with
“YY” the last two digits of the production year, “MM”
the production month and “DD” the production day),
the Application Identifier (21) the serial number of the
device (“WWWWWWWWW”) if applicable, and the
Application Identifier (10)ZZZZZZ the lot number of the
device (“ZZZZZZ”) if applicable
Type BF applied part (patient isolation from electrical
shock)
In compliance with the European Directive on Waste of
Electrical and Electronic Equipment (WEEE) 2002/96/EC,
do not dispose of this product as unsorted municipal
waste
Non ionizing radiation. Equipment includes RF
transmitter: interference may occur in the vicinity of
equipment marked with this symbol
Federal Communications Commission (FCC) logo
CE marking indicating conformance to EC directive
93/42/EEC and 2007/47/EC concerning medical devices
Contains TX IC: 1520A-LMX9838
Industry Canada (IC) label