Symbols
Follow instructions for use. (Symbol appears blue on product labeling.)
Equipment includes RF transmitter
Affixed to this device in accordance with European Council Directive
2002/96/EC.
These directives call for separate collection and disposal of electrical and
electronic equipment. Sorting such waste and removing it from other forms
of waste lessens the contribution of potentially toxic substances into
municipal disposal systems and into the larger ecosystem.
Confirmite Europeenne (European Conformity). Affixed in accordance with
European Council Directive 93/42/EEC (NB 0086) and R&TTE Directive
1999/5/EC and 2011/65/EU. Hereby, St. Jude Medical declares that this
device is in compliance with the essential requirements and other relevant
provisions of this directive
FCC identifier for the transmitter
IC identifier for transmitter
This device complies with part 15 of the FCC Rules and RSS-210 of the IC
Rules. Operation is subject to the following two conditions: (1) This device
may not cause harmful interference, and (2) this device must accept any
interference received, including interference that may cause undesired
operation.
Denotes compliance with AS/NZS standards: AS/NZS 4268:2003
Australian Communications and Media Authority (ACMA) and New Zealand
Radio Spectrum Management (RSM) Regulatory Compliance Mark (RCM)
Japanese RF identifier for the transmitter
cETLus valid for Canada and US Classified
Conforms to UL 60601-1.
Certified to CAN/CSA STD C22.2 NO 601.1 –M90
Serial number
Unit ready for use
Unit not ready for use
Caution
Defibrillation-proof Type CF equipment
Only connect specified power supply equipment
Manufacturer
11