Why paper on one side?

Medical sterilisation paper is gas-permeable but microbe-tight. Ethylene oxide or steam reach the product while micro-organisms cannot pass back. Without that permeability a sealed pouch could not be sterilised.

Do the pouches meet ISO 11607?

ISO 11607 sets requirements for sterile barrier systems and their validation. Conformity must be demonstrated by the medical device manufacturer for the specific combination of material, process and product. The machine is a prerequisite, not the evidence itself.

What does peelable mean?

A peelable seal opens in a controlled, fibre-free way. This matters so that no paper fibres are released during opening in the sterile field and the product can be presented aseptically.

Which sterilisation methods are possible?

That depends on the material used. Ethylene oxide and steam sterilisation are common. Suitability for a given method follows from the material specification of the film and paper supplier.

DLP-600 Medizin Papier/Kunststoff

DLP-600 Medical: paper-plastic sterile pouches

The DLP-600 Medical produces 3-side-seal pouches from paper/paper and paper/plastic laminates for the sterile packaging of medical devices. The paper side lets sterilisation media such as ethylene oxide or steam pass through, while the plastic side stays transparent for visual identification.

Category: Medical
Technology line: Classic line

Request a quote for DLP-600 Medizin Papier/Kunststoff Get in touch

Bag formats

Paper/plastic sterile pouches
Paper/paper sterile pouches
3-side-seal pouches for medical devices

Materials

Medical sterilisation paper
PET/PE viewing films
Paper/plastic laminates

Applications

Single-use instruments and theatre accessories
Catheters, cannulas and syringes
Wound care products
Dental instruments
Sterile supply in hospitals

What defines this machine

Paper side as sterilisation barrier

Medical sterilisation paper is gas-permeable but microbe-tight. Ethylene oxide or steam reach the product, micro-organisms do not travel back. That is the basic principle of a sterile barrier system.

Viewing side for content identification

The transparent plastic side allows identification without opening. In theatre operation that is a question of time and safety.

Uniform seal as an inspected feature

On sterile barrier systems the seal is safety-relevant and inspected. Constant sealing parameters across the whole batch are therefore a basic requirement, not merely a quality target.

Peelable version possible

With suitable material combinations the seal can be designed to open fibre-free, which is required for aseptic presentation in the sterile field.

Technical data

DLP-600 Medizin Papier/Kunststoff: Technical data
Material combinations	paper/paper, paper/plastic
Bag type	3-side seal
Bag width	on request
Bag length	on request
Output rate	on request
Max. film width	on request
Max. reel diameter	on request
Connected load	on request
Compressed air	on request
Machine dimensions (L × W × H)	on request
Weight	on request

Numerical values are confirmed by the factory for your application. We supply the full data sheet with the quotation.

Frequently asked questions

Why paper on one side?: Medical sterilisation paper is gas-permeable but microbe-tight. Ethylene oxide or steam reach the product while micro-organisms cannot pass back. Without that permeability a sealed pouch could not be sterilised.
Do the pouches meet ISO 11607?: ISO 11607 sets requirements for sterile barrier systems and their validation. Conformity must be demonstrated by the medical device manufacturer for the specific combination of material, process and product. The machine is a prerequisite, not the evidence itself.
What does peelable mean?: A peelable seal opens in a controlled, fibre-free way. This matters so that no paper fibres are released during opening in the sterile field and the product can be presented aseptically.
Which sterilisation methods are possible?: That depends on the material used. Ethylene oxide and steam sterilisation are common. Suitability for a given method follows from the material specification of the film and paper supplier.