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Clean room doors and health care

Our cleanroom division is there to provide you with its expertise and to support you in your automation projects. We have developed a very wide range of technical solutions, which allows us to respond with relevance.

This expertise and range of solutions have enabled us to build a well-established reputation internationally, particularly in the fields of laboratories, health care, production industries and logistics areas.

Sliding doors

HDS CLEAN hermetic door

Airtightness in operating theatres

100% airtight up to 25 Pa
HPL solid panel with or without oculus
PV air permeability CSTB BV12035
NF EN1026

HDS Clean X-ray door

X-ray protection in X-ray rooms

HPL lead shielded solid panel with or without x-ray oculus
Personnel safety
NF EN1026

Diva L Clean

Portes étanches dans un hôpital à Clermont-Ferrand

Controlled leakage rate
Airflow control
G25 glazed or solid sash HDS Clean
PV air permeability CSTB BV11-811/B BV11-811/A1
EN 61000-6-2

Our assets

We are able to intervene at all stages of your projects: study, design, custom production, installation and maintenance of your automatic doors.

Our design offices will work with you to qualify the technical solutions that will meet your specifications.

Whether it is a question of controlling atmospheric conditions, resistance to pressure differences, asepsis, operating intensity, protection against shocks, compliance with standards, or safety of people and property, we choose the most suitable processes and materials.

Finally, our staff is certified to carry out installation or maintenance operations in high-risk areas.


The standards

Today Portalp offers you certified doors that meet the most stringent requirements.

ISO Standard – 14644-1
(Particulate and chemical contamination)

This certification specifies the classification of the particulate cleanliness of the air.

The maximum permissible concentrations of particles are in classes ranging from ISO 1 (most stringent class) to ISO 9.

Standard ISO – 14698-1
(Microbiological contamination)

Specific to the pharmaceutical industry, this standard, dedicated to the control of biocontamination, deals with the monitoring methods to be used according to the medium/fluid.

The dust classifications are defined according to the criticality of the activity.

The tolerance in concentration per m3 of air in dust and micro-organisms contaminants is organized in classes from A (for high risk areas) to D (for less critical areas with controlled atmosphere).