Food / Pharma
When manufacturing of food products, additives, and pharmaceutical agents, you fulfill the most stringent requirements for product purity. You can rely on your partner Kayser Filtertech for separating solids and liquids and removing dust. Find the perfect solution for each specific filtration application—efficient, safe, and sustainable.
Kayser filter media are:
- Chemically resistant
- Thermally resistant
- Mechanically resistant
- Electrically conductive
- Very selective, with high separation performance
- Reliably regenerable
- Suitable for food products (EU VO 10/2011 and FDA CFR 21 §177)
- Available in GMP versions
food.STAR by Kayser Filtertech
Filter elements that conform to EU and FDA standards for contact with food products
- Recognized materials:
Our filter media are made of positively listed materials.
- Migration targets:
Independent testing institutes regularly test for compliance with overall migration limits. A look at the chart shows that our filter media are as much as 30 times less than the limits.
- Production processes
Kayser filter elements are produced in accordance with GMP and HACCP standards. They can be integrated in food product processes in a safe, compliant manner, including conveying, milling, drying, and dehydrating. Operating temperatures up to 250 °C.
- Declared conformity
Filter elements are available with conformity declaration per EU directive 10/2011 (includes the consumer goods directive) and per FDA CFR 21 §177 upon request. Legally conforming filter media fulfill the requirements of ISO 22000 and IFS 5.
Kayser Filtertech products provide:
- High operational reliability
- Reduced emissions
- High product yields
Areas of application
Pharmaceutical and chemical industry:
- Titanium dioxide
- Aluminum oxide
- Lead and iron oxide
- Specialty pharmaceutical products
Food products industry
- Powdered milk
- Animal feed
- Instant powders
Filter elements for the pharmaceutical industry
Reliable processes—sterile packaging
Sterile packaged filter elements from Kayser are used wherever process reliability demands the most stringent requirements. All sterilization methods used are based on proven methodologies, such as those used for sterilizing surgical instruments.
Safety through conformity
The amount of extractable components is very low. The basis for pharma conformity is the requirements of the EU and FDA. In addition, the concentration of the following substances is below detectable limits:
- Bisphenol A
- Heavy metal (Cd, Cr, Hg, Pb)
- Chlorinated hydrocarbons
Consistency and efficiency
Depending on the design, our sterile packaged filter elements can be used at temperatures of up to 250 °C and pH levels from 1–14. Available materials include PP, PET, PPS, and PTFE.
Ultrafine particles (< 1 µm) are separated out by an inert PTFE membrane.
Audited processes, traceable products
The production processes at Kayser Filtertech have been audited multiple times by pharmaceutical companies. These including globally active corporations. Every filter hose can be labeled without ink upon request in order to ensure 100% traceability.