VertiBaX registered with the MHRA
VertiBax is registered with the Medicines and Healthcare products Regulatory Agency to manufacture Class 1 Medical Devices which includes orthopaedic support devices and postural support devices.
The MHRA is an executive agency of the Department of Health with the sole purpose of safeguarding public health. By registering with this organisation VertiBaX can offer the guarantee that all products manufactured by them have been done so in accordance with the European Council Directive 93/42/EEC of 14 June 1993 concerning medical devices. To demonstrate this all VertiBaX products carry the CE marking. For more information visit www.mhra.gov.uk
16/04/2007
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