SGS Certification Statement

Where a product manufactured by Schottlander is shown as having been certified as a medical device in the European Union under the Medical Device Directive 93/42/EEC by SGS CE0120, this is exclusively for the indication(s) shown in the Instructions for Use of the product concerned. Other non-medical uses ascribed to this device are not within the scope of CE certification, and users should be aware that product performance and/or safety has not been evaluated by SGS for those purposes.