The Electronic Health Record software (Class I) and the PACS system (Class IIa) are medical devices classified under the UK Medical Devices Regulations 2002 (as amended).
SThey carry a CE mark indicating compliance with the regulations.
The content on this site is intended solely for qualified healthcare professionals. Pre-certification modules are provided for evaluation purposes only and are not UKCA or CE certified.
For detailed performance and usage instructions, refer to each product's technical documentation.

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