- Hong Kong
- New Zealand
- Saudi Arabia
- South Africa
- United Arab Emirates
- United Kingdom
- United States
SEERS Medical are accredited to the ISO 13485:2016 Quality Management System for Medical Devices. This specifies the requirements for the design, manufacture and support of products. SEERS Medical are currently certified up to 2023 but the certificate will be renewed before expiration.
SEERS Medical products comply with the Essential Requirements in Annex I of EC Directive 93/42/EEC, with all relevant design, production records, risk assessments, product testing and labelling information recorded in the documentation file labelled the “Technical File”. All products lift the rated Safe Working Load smoothly from the minimum height to the maximum height and are tested to 2.5x the safe working load for over an hour, to prove load support capacity. This is in accordance to EN60601:2006.
Upholstered sections comply with flammability requirements of BS 7176:1995 (medium hazard) using ignition sources 0 (cigarette) and 1 (gas) defined in BS EN 1921-1 2,5 (crib) BS 5852:1990.
All SEERS Medical treatment couches, manufactured during or after September 2017, feature a lifetime frame warranty and a five year warranty on all other components.
All SEERS Medical products comply to EN 60601- 1:2006+A12:2014 (E) the General requirements for basic safety and essential performance. In addition, the actuation and control systems used on our products are marked with the UL mark, demonstrating compliance to UL60601-1 and CAN/CSA-C22.2 No. 601.1-M90, meeting the requirements for USA and Canada. The actuation control system is also marked with approval to C-ETL-US No. 3154358.