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Aseptic PET filling equipment with dry preform sterilisation

Sidel announces approval of its aseptic Combi Predis blow fill seal filler for low acid product manufacturing in the U.S.


Sidel has received Food and Drug Administration (FDA) approval for its Aseptic Combi Predis™ FMa blow fill seal filler following tests run at a dairy customer in North America. This means that the Sidel Aseptic Combi Predis FMa PET filler is validated for low acid manufacturing and commercial distribution in the United States market. The Sidel Aseptic blow fill seal solution is the world's first aseptic PET filling equipment with dry preform sterilisation approved by FDA.

Sidel has received Food and Drug Administration (FDA) approval for its Aseptic Combi Predis™ FMa blow fill seal filler following tests run at a dairy customer in North America. This means that the Sidel Aseptic Combi Predis FMa PET filler is validated for low acid manufacturing and commercial distribution in the United States market. The Sidel Aseptic blow fill seal solution is the world's first aseptic PET filling equipment with dry preform sterilisation approved by FDA. 

"We are particularly proud of this FDA acceptance", explains Guillaume Rolland, Sensitive Products Director at Sidel. "It confirms our Aseptic Combi Predis design is compliant with the FDA's current Good Manufacturing Practice (cGMP) requirements." This FDA approval officially qualifies the Sidel aseptic solution with dry preform sterilisation technology to produce and distribute shelf-stable low acid products in PET bottles for the US market.

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