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Validatable rotary sealer for medical packaging of sterilization pouches
We are more than willing to support you with your request or run a demo with your packaging.
The D 662 MV produces a 12,5 mm multiline validatable seal, fully compatible with sealing requirements of EN 868-5, DIN 58953-7 and validation requirements of ISO 11607-2 and ISO/TS 16775.
This rotary sealer is equipped with an epoxy housing and stainless steel upper cover for hygienic cleaning. The digital and simple keyboard allows you to easily set and monitor the critical process parameters like seal temperature, seal force and seal speed. All critical process parameters are traceable and can be exported to a USB for logging.
This rotary sealer is suitable for sealing medical pouches such as pre-made sterile barrier systems (EN 868-5), Uncoated synthetic (medical) paper and thin paper laminates. Not suitable for sealing Polyethylene pouches.
To optimize your user convenience and packaging performance, this machine comes standard with an easy-to-clean stainless steel work table that supports your packages during the seal process.
This ensures a straight seal while the operator's hands remain available to feed the next package to the machine, saving time.
To sum up:
The Contimed D 662 MV gives you as an end-user the following benefits:
The following options are available on the Contimed D 662 MV (work table is already included):
Please see below more specifications of the Contimed D 662 MV:
We work together with you in providing the best quality packaging machines to help you grow your business.
This model is operated by means of a user-friendly digital panel, enabling you to program the optimum packaging settings. This enables a consistent and reliable packaging result while saving production time and reducing product failure.
The validatable D 662 MV can be deployed in sterile environments and cleanrooms to perform consistent, reliable packaging productions. Its robust housing is easy-to-clean including the digitial membrane control panel.
Control and monitor all process parameters, such as seal temperature, seal force and speed. In addition to the provided seal quality guarantee, you are further assured of compliance with the requirements/regulations for your products in your specific industry by means of traceble validation.
The integrated alarm feature will inform you when the seal temperature is outside of tolerance (+/- 5°C). By having consistency on your production batches you remain assured of the best packaging quality that follow the set requirments of your field.
Audion offers a wide range of instruments and solutions that enable users to test and verify their packaging machines and seals, in order to meet the high market demands. These include:
Seal Integrity Test (SIT) as a service which includes:
Other related solutions to fit your needs:
Audion provides professional calibration services for our validatable sealers. The critical process parameters (seal temperature, seal force, seal time, cooling temperature) are measured with traceable measuring devices and a calibration certificate will be issued.
Installation qualification (IQ) and Operational qualification (OQ) scripts are mandatory within the pharma/medical industry due to the high-quality sealing demands. Our team of experts will conduct multiple tests with different scenarios with your pouches to determine that our machine complies to the necessary packaging demands.
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Do you want to know what the Contimed D 662 MV can offer for your company? Please feel free to contact us as we are looking forward to explore together which packaging solution will benefit you most.
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Audion
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