The hygienic design and customer-specific special features of the Vakulab® HL handle the demanding tasks involved in the production of sterile materials, such as solutions or filled syringes, as well as those encountered in production-related areas where the sterilization of fermenters, machine parts, clean room garments, filters, etc. calls for individual solutions.
Our response to the pharmaceutical industry’s strict demands for design and process reliability.
Suitable for sterilizing solid and porous materials using the pre-vacuum process or pulsed vacuum process following by drying. Liquids in open or loosely sealed containers using the pre-vacuum process.
Liquids in tightly sealed containers made from glass or heat-resistant material using the steam/air mixture method (SAMM) (only with the steam/air mixture process option). Infectious materials (only with the Exhaust air filter feature). The sterilizer complies with the Pressure Equipment Directive (PED) 2014/68/EU and the Machinery Directive 2006/42/EC. CE marking according to PED 2014/68/EU. The standards applied are: DIN 58950, AD 2000 Design of Pressure Vessels and DIN EN 62304 Medical device software.
Siemens controller
12” or 15” display, or customer-specific size
Clamp or aseptic threaded connections
FDA-compliant sealing materials and lubricants (21 CFR)
F0 value controlled process sequence
Filter housing and elements can be sterilized inline
Active jacket cooling
Recirculation cooling and cooling circuit connection
Cooling coil
Sterile filtration of compressed air
Air detector
Air-tight separation
Fan for steam/air mixture process
“Closed solutions” equipment package