News ¦ IDM
Aseptic Combi Predis
Sidel celebrates three years of FDA validation
In 2017, the Sidel Aseptic Combi Predis blow fill seal filler was validated
by the American Food and Drug Administration (FDA) for
low acid products sold in the US – an industry first. With more
than 180 references at major beverage and dairy companies since
the launch of this safe and simple solution in early 2000, the repeated
orders recorded by this technology underline its success.
The Aseptic Combi Predis differs from former aseptic bottling
technologies because the PET package sterilisation already
takes place at the preform stage rather than during
the bottling phase. The solution marks an important step towards
a sustainable production because it does not require
any water and uses only a minimal amount of chemicals: its
blower oven activates the sterilising effect of the hydrogen
peroxide (H2O2) vapour, thus eliminating the need for additional
heating of the preforms, saving further on resources.
The dry preform sterilisation before the oven prevents recontamination
and avoids the need for blow moulder sterilisation.
It also eliminates the constraints related to the bottle
shape’s complexity. Therefore, the solution is able to handle
bottle formats from 200 ml to 3 L with any shape. For greater
flexibility, format changeovers are easy and fast, taking only
one minute per mould. In its latest generation – the Versatile
Aseptic Combi Predis – the solution is even able to manage still
beverages and carbonated soft drinks in PET on one piece of
equipment. sidel.com
Sidel celebrates 3 years of FDA validation for its Aseptic
Combi Predis (Photo: Sidel)
Dosing Fill in g Packi n g
UF WHITE CHEESE cup filling line
the modern technology of the GRUNWALD filling, coagulation and closing line
for producing and filling different types of UF white cheese into ready-made plastic cups
GRUNWALD GMBH · Pettermandstr. 9 · 88239 Wangen im Allgäu/Germany · Phone +49 7522 97050 · info@grunwald-wangen.de · www.grunwald-wangen.de
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/sidel.com
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