Product

KS Seal

Airtight waste containment at the point of preparation.

Sealed waste containment at the point of preparation, with a functional foil cassette.
KS Seal
Configured to the workflowSet up for the preparation in scope, not a generic installation.
Software-guided stepsOrder entry, calculation and guided preparation.
KAPSAM sterile disposablesFluid paths produced in ISO 14644 compliant cleanrooms.
Installation and serviceCommissioning, user training and technical support.
Overview

What this product does

KS-Seal contains waste generated during preparation close to the point where it arises, using an airtight foil cassette that minimises cross-contamination before material leaves the controlled area.

Benefits

Designed around the workflow

Advanced safety

Airtight sealing contains material at the point of use.

User-friendly design

Operation fits the preparation routine rather than interrupting it.

Mobile and versatile

Height-adjustable between 96 and 120 cm for different room layouts.

Functional foil cassette

Provides a repeatable, consistent sealing method.

Minimise cross-contamination

Waste is isolated before transfer out of the controlled area.

In action

Positioned within the preparation area so that waste handling does not interrupt the compounding workflow.

KS Seal waste containment
Software

Workflow software and connectivity

No dedicated software scope.

Consumables

Related sterile components

Technical

Specification and regulatory information

WeightApproximately 45 kg
Dimensions (w x d x h)52 x 48 x (96-120) cm

Regulatory status and certification are published once Quality review is complete.

Request information on KS Seal

Documents

Brochures, certificates and technical information

Product documents available to download.

ISO, CE and conformity documentation.

Ask for the documentation released for your market.

Questions

Frequently asked questions

The answers below cover what hospital pharmacy, IT and technical teams ask most often. If your question is not here, our team will answer it directly.

Does the system integrate with our hospital information system?

Yes. KAPSAM systems exchange order and preparation data with HIS/EHR environments through HL7 and API integration, scoped per project with your IT team.

Which consumables are used with the system?

KAPSAM manufactures the sterile disposables used in the fluid path, including EVA bags, IV lines, filters and administration sets, assembled and sterilised in ISO 14644 compliant cleanrooms.

What training and service is provided after installation?

Installation and commissioning, on-site or virtual user training, preventive maintenance and technical support are provided by the KAPSAM service team or a trained distributor partner.

Which certificates are available for the product?

KAPSAM operates ISO 13485:2016, ISO 9001:2015 and ISO 14001:2015 certified systems and is audited by a notified body (CE 0425). Certificates can be downloaded from the Quality page.

Discuss this product with our team

Tell us about your application area, preparation volume and hospital systems. We will respond with the relevant technical and project information.