Pharmaceutical Pump Sealing Solutions

– Effectively prevent leakage and pollution, ensuring production safety.

Specifically tailored for pharmaceutical processes, resistant to corrosion, capable of CIP/SIP cleaning, and compliant with FDA and USP VI standards.

В пищевой промышленности и производстве напитков механические уплотнения играют важнейшую роль в обеспечении гигиены, предотвращении загрязнения и поддержании эффективности технологического оборудования. Эти уплотнения должны соответствовать строгим нормам безопасности пищевых продуктов, выдерживать воздействие чистящих химикатов и надежно работать в диапазоне температур и давлений. Компания Sakowitz предлагает высокопроизводительные механические уплотнения, разработанные специально для применения в пищевой промышленности и производстве напитков, обеспечивающие безопасность, долговечность и соответствие отраслевым стандартам.

680 Metal Bellow Mechanical Seal

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Типы механических уплотнений для фармацевтической промышленности

  • Гигиенические механические уплотнения — Comply with food-grade and pharmaceutical-grade hygiene standards.
  • Single Mechanical Seals — Commonly used in ordinary conveying pumps.
  • Dual Mechanical Seals — Suitable for high-purity media, sterile equipment, and hazardous materials.
  • Картриджные механические уплотнения — Reduce installation errors and enhance sterility stability.
  • Металлические сильфонные уплотнения — Suitable for high-temperature sterilization and strong corrosive cleaning agents.
  • Уплотнения с сухим ходом — Sterile processes in dry environments.
  • FDA & USP VI Certified Seals — Used in critical pharmaceutical equipment.

WHY USE IT

Why Mechanical Seals Matter in Pharmaceutical Production

  • Prevent cross-contamination and ensure the purity of the drugs.
  • Adapt to CIP / SIP (in-situ cleaning / in-situ sterilization).
  • Withstand disinfectants, high-temperature steam, and corrosive cleaning solutions.
  • Reduce leakage → Prevent material loss and avoid microbial contamination.

Pharmaceutical & Biochemical Industry

Material Requirements for Pharmaceutical Pump Seals

Sakowitz Certificates

The pharmaceutical industry has strict requirements for materials. All sealing materials must be safe, stable, and comply with pharmaceutical production regulations. The following are the core requirements:

  • Металлические компоненты
    Use SS316L or Hastelloy. These materials have excellent corrosion resistance and comply with the specifications for metal release and hygiene standards in pharmaceutical production.
  • Эластомеры
    Use materials such as EPDM, FFKM, and FDA-grade FKM. All have passed FDA и USP Class VI standards, ensuring no harmful substances are released.
  • Лицевые стороны печатей
    Choose SiC, Carbon, and Ceramic. These materials are stable and do not cause particle shedding, thus avoiding the risk of contaminating the liquid medicine.
  • Surface Finish Require Ra < 0.4 μm.
    The smoother the surface, the more it can reduce microbial adhesion and facilitate the implementation of CIP/SIP cleaning procedures.

Recommended Seal Models for Pharmaceutical Applications

The following models have been specifically developed for the pharmaceutical industry to meet the requirements for sterile, safe, and cleanable processes:

ModelApplication / Description
XD301-HSuitable for sterile pumps, dairy pumps, and purified fluid transfer. Designed with a hygienic structure, easy to clean, and compliant with FDA and USP Class VI standards.
XD169-SDesigned for CIP/SIP cleaning and sterilization processes. Resistant to high temperatures and cleaning chemicals; commonly used for circulation and transfer pumps.
XD7P-FDAIdeal for medium- to high-viscosity fluids such as bioproducts, fermentation liquids, and nutraceuticals. Provides stable sealing, reduces product residue, and improves sanitary performance.

Key Industries & Application Scenarios for Pharmaceutical Sealing Solutions

Sterile Processing
Sterile Processing

Equipment for aseptic filling, sterilisation, and pre-treatment of water for injections. Sealing must be hygienic grade with no dead corners, supporting CIP/SIP to ensure the sterile environment remains uncompromised.

Biopharmaceutical Production
Biopharmaceutical Production

Suitable for fermenters, bioreactors and purification equipment. Sealing materials must exhibit low migration and be free from particle shedding to ensure no contamination of active substances.

Vaccines & Biotechnology
Vaccines & Biotechnology

Meeting the requirements for high cleanliness and corrosion resistance, it maintains a stable seal throughout cell culture, virus inactivation, and filling processes.

Oral Liquid Production
Oral Liquid Production

For use in syrup pumps, clean medium transfer pumps, etc. The seal must withstand high-temperature sterilisation to ensure the product remains isolated from external contamination.

API Synthesis
API Synthesis

Suitable for chemical synthesis processes such as reaction vessels and solvent pumps. Requires mechanical seals with high corrosion resistance and thermal stability, suitable for media including acids, alkalis, and organic solvents.

Nutraceuticals
Nutraceuticals

Suitable for materials such as protein powder, nutritional solutions, and plant extracts. Sealing must be easy to clean, food-grade, and free from cross-contamination risks.

WHY CHOOSE US

Why Partner with Sakowitz

Over 30 years of sealing research and development experience

Customers in over 50 countries worldwide

Provide FDA, USP VI, and 3-A certification materials

CNC precision < 2 μm

Can replace John Crane / EagleBurgmann / Flowserve

Complete technical support and rapid delivery

FAQ – Pharmaceutical Pump Sealing Solutions

Q1: Do your seals comply with the requirements of the FDA and USP Class VI?

Yes. We can offer FDA-compliant elastomers and materials that have passed USP Class VI testing and certification, which are suitable for aseptic and pharmaceutical-grade applications.

Sure. The sealed structure supports steam sterilization at 120-150°C and can withstand common cleaning chemicals, making it suitable for continuous CIP/SIP processes.

It is usually 2 to 4 years. The exact lifespan depends on temperature, cleaning frequency, medium pH value and the operating mode of the equipment.

Sure. We offer full-size customized services including non-standard shaft diameters, special materials, sanitary-grade structures, and low-residue designs.

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