Medical autoclave Vakulab® HL
for the pharmaceutical industryhorizontal

Medical autoclave - Vakulab® HL - MMM Group - for the pharmaceutical industry / horizontal
Medical autoclave - Vakulab® HL - MMM Group - for the pharmaceutical industry / horizontal
Medical autoclave - Vakulab® HL - MMM Group - for the pharmaceutical industry / horizontal - image - 2
Medical autoclave - Vakulab® HL - MMM Group - for the pharmaceutical industry / horizontal - image - 3
Medical autoclave - Vakulab® HL - MMM Group - for the pharmaceutical industry / horizontal - image - 4
Medical autoclave - Vakulab® HL - MMM Group - for the pharmaceutical industry / horizontal - image - 5
Medical autoclave - Vakulab® HL - MMM Group - for the pharmaceutical industry / horizontal - image - 6
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Characteristics

Applications
medical, for the pharmaceutical industry
Configuration
horizontal
Capacity

460 l, 644 l
(121.52 gal, 170.13 gal)

Width

1,900 mm
(75 in)

Height

1,918 mm
(75.5 in)

Depth

1,360 mm
(54 in)

Description

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

Exhibitions

Meet this supplier at the following exhibition(s):

ArabHealth 2025
ArabHealth 2025

27-30 Jan 2025 Dubai (United Arab Emirates) Stand H3.C31

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    *Prices are pre-tax. They exclude delivery charges and customs duties and do not include additional charges for installation or activation options. Prices are indicative only and may vary by country, with changes to the cost of raw materials and exchange rates.