5Symbols interpretationSafety Test Standards: Medical Devices Directive 93/42/EEC IEC 60601-1:2005+A1:2012/EN 60601-1:2006 Medical electrical equipment - Part 1: Generalrequirements for basic safety and essential performance IEC 60601-1-2:2007/EN 60601-1-2:2007 Medical electrical equipment - Part 1-2: Generalrequirements for safety - Collateral standard: Electromagnetic compatibility - Requirements andtests IEC 60601-2-10:2012/EN 60601-2-10:2000+A1:2001 Medical electrical equipment - Part 2-10:Particular requirements for the safety of nerve and muscle stimulators IEC 60601-1-11:2010 Medical electrical equipment -- Part 1-11: General requirements for basicsafety and essential performance -- Collateral standard: Requirements for medical electricalequipment and medical electrical systems used in the home healthcare environment. EN 980 Symbols for use in the labeling of medical devices EN 1041 Information supplied by the manufacturer with medical devices IEC/60601-1-6/ EN 60601-1-6 Medical electrical equipment – Part1-6: General requirements forbasic safety and essential performance – Collateral standard: UsabilityFragile, handle with care Type BF applied partKeep the product in the dryplaceAway from water and rain.CAUTION, Avoid injury.Read and understand owner’smanual before operating thisproduct.This way up ManufacturerProduct package should berecycled.Symbol for "AUTHORISEDREPRESENTATIVE IN THEEUROPEAN COMMUNITY"Unrecyclable Batch codeDate of manufacture FDA510(k) FDA 510(k) clearedSerial number IP22 IP code of the device