APC

Available Sizes       : 1",1½" ,2",2½", 3" , 4",5" .
Available Materials : Buna-N (gray), Buna-N (Black),E.P.D.M ,Viton® Black
                                      Silicone Platinum (Clear),Tefon®
Certifications          : 3 A, FDA.

Inline Validation Spore Trap Gaskets

•  Description : The Spore Trap is designed to securely retain and accurately expose spore challenge test strips for use in steam sterilization when validating. After each validation cycle, the spore trap, with its securely retained test strip can easily be removed and rechallenged.
Available Sizes : 1,50"-2,00"-2,50"-3,00"-4,00"
•  Material : Platinum Cured Silicone
•  Certifications : FDA- USP Class VI

Pressure Gauge Isolator

•  Description : Gauge Guard Isolator gaskets protect expensive diaphragms and instruments from damage without affecting instrument performance
Available Sizes : 0,75"-1,00"-1,50"-2,00"
•  Material : Platinum Cured Silicone - Viton -EPDM
•  Certifications : FDA- USP Class VI

Gauge Guard Protector

•  Description : Combine the Gauge Guard Protector with a quality Gauge Guard Isolator Gasket to achieve complete diaphragm protection.
A necessary and cost effective step in assuring maximum service life and accurate results from your instruments and gauges
Available Sizes : 0,75"-1,00"-1,50"-2,00"
•  Material : Platinum Cured Silicone and 316SS
•  Certifications : FDA- USP Class VI

Smart Gaskets

•  Available Sizes : 0,50"-0,75"-1,00"-1,50"-2,00"-2,50"-3,00"-4,00"-6,00".
Ports : 1, 2, 3 and 4 internal ports available
•  Tolerances : Thermocouple Clamp,Spore Trap,Sampling Valve
•  Material : EPDM, platinum-cured silicone, and FKM
•  Certifications : FDA -USP Class VI
FDA BONDED ORIFICE PLATES FDA CLASS VI MINI ORIFICE PLATE GASKET REMOVABLE FDA ORIFICE PLATES SOLID TRI-CLAMP FDA GASKET Logo FDA iso flag

 

 

 

 

The Role of the Sanitary Standards

All of the criteria lead to a design in which every product contact surface that can be touched by product will also be in contact with cleaning solutions at the proper temperature and flow rate so that all product residues are removed.This would seem to imply that all equipment meeting a 3-A Sanitary Standards or Accepted Practices is suitable for CIP cleaning.