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DEAR CUSTOMER, thank you for choosing a GLOBUS product. We reamain
at your entire disposal for any assistence or advice you may need.
The device has been manufactured in compliance with applicable
technical regulations and has been certified in compliance with Directive
93/42/EEC as amended by 2007/47 Directive for medical devices, by
Kiwa Cermet Italia S.p.A. Body n. 0476, in order to ensure product safety.
ENGLISH
Rev. 03 Multi_06_2018
Summary of Contents for DUO TENS
Page 16: ...16 MODO D USO Rev 03 Multi_06_2018...
Page 36: ...36 Rev 03 Multi_06_2018...
Page 50: ...50 INSTRUCTIONS FOR USE Rev 03 Multi_06_2018...
Page 70: ...70 Rev 03 Multi_06_2018...
Page 84: ...84 INSTRUCCIONES DE USO Rev 03 Multi_06_2018...
Page 104: ...104 Rev 03 Multi_06_2018...
Page 118: ...118 MODE D EMPLOI Rev 03 Multi_06_2018...
Page 139: ...139 Rev 03 Multi_06_2018...
Page 148: ...148 Rev 03 Multi_06_2018 DOMINO S R L Via Vittorio Veneto 52 31013 Codogn TV Tel 39 0438 7933...