Table 50. Symbols and definitions
Catalog number
Manufacturer
Contents quantity
Pulse generator
Accessories
Serial number
Batch code
Unique Device Identification
Prescription use only
Ethylene oxide gas sterilization
Authorized European representative
European conformity, affixed according to the relevant provisions of AIMD
directive 90/385/EEC and RE directive 2014/53/EU Annex II. Hereby, Abbott
Medical declares that this device complies with the essential requirements and
other relevant provisions of these directives.
The full text of the European Union RE directive 2014/53/EU declaration of
conformity is available at the following internet address:
www.neuromodulation.abbott/euconformity.
Australian Communications and Media Authority (ACMA) and New Zealand
Radio Spectrum Management (RSM) Regulatory Compliance Mark (RCM)
This equipment is certified for type certification pursuant of Article 38-24 of the
Japan Radio Law
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