Certified Hermetic Doors for Singapore Hospitals

Frameshft hermetic doors are certified to BS EN1026:2000 and BS EN12207:2016 for air permeability and classification, with CE marking under the LVD Directive and TÜV verification. These certifications are commonly required for hospital procurement submissions and infection control compliance documentation. Each system also carries a failsafe motor lock that engages on power interruption. Full certification documentation is provided with every installation to support your facility's compliance records.

Yes. Frameshft hermetic doors are specifically engineered to support air pressure differentials, which are a standard requirement in operating theatres and ICUs. The airtight seal construction, flush anodised aluminium edging, and sealed panel integration maintain the pressure boundary at the entrance. This is validated through BS EN1026:2000 certification, which tests air permeability under defined pressure conditions.

Frameshft hermetic door leaves are rated up to 1,000kg. This accommodates the additional mass required for the flush panel construction, sealed edging, and acoustic layering that deliver STC35 sound attenuation alongside airtight performance. The 40V 100W German Dunkenmotoren drive unit with integrated motor lock is specified to handle this load reliably across a clinical high-cycle environment.

Frameshft's multi-brand repair and servicing capability covers most automatic door operator brands, not only Frameshft systems. If your facility has existing hermetic or other automatic doors from a different supplier, our technical team can assess, service, and maintain them under a single service agreement. This consolidates your FM team's door servicing into one point of contact, reducing coordination overhead across a mixed installed base.

Yes. While Frameshft's hermetic door systems are most commonly specified for hospital operating theatres and ICUs, the same airtight seal engineering, pressure differential support, and certification stack are applicable to cleanroom and pharmaceutical manufacturing environments where contamination control and sterile integrity are required. Our technical team can assess your specific environment requirements during the initial site consultation.