PH 50 - PH 4000 Pharmadry®
Vacuum Paddle Dryers
The Pharmadry® vacuum paddle dryer with short drying times is well suited for the drying of freely flowing, sensitive pharmaceutical ingredients and fine chemicals. Designed to meet stringent cGMP and FDA guidelines
Agitator supported at the rear, with externally exchangeable mechanical seal. Designed for frequent product changes. Excellent cleanability using CIP Systems, simple validation.
Good product discharge characteristics with negligible product residues, due to narrow agitator to wall clearances, minimal vessel depth and a special agitator blade design.
Special properties for the customer's benefit
Calculation, design and manufacture in compliance with Pressure Equipment Directive 97/23/EG or/and ASME U-Stamp as well as with cGMP and FDA guidelines
EG type examination certification 03ATEX0246X in accord with PED 94/9/EG or with UL-approved electrical components for operations in class 1, division 1 or 2, group C & D environment
Double mechanical seal, externally interchangeable, non-contacting gas-lubricated (lift-off), dry running contact (contacting sliding surfaces) or liquid-lubricated seal
Sampler valve
Pre-piping made of stainless steel on terminal box
Excellent cleanability using CIP-systems, simple validation
Options
Pressure-resistant and sterile versions, isolators (glove box), DQ, IQ, OQ qualification
Autonomic PLC control or connected to PMSX, heavy current box
PH 50 - PH 4000 Pharmadry®
Vacuum Paddle Dryers
The Pharmadry® vacuum paddle dryer with short drying times is well suited for the drying of freely flowing, sensitive pharmaceutical ingredients and fine chemicals. Designed to meet stringent cGMP and FDA guidelines
Agitator supported at the rear, with externally exchangeable mechanical seal. Designed for frequent product changes. Excellent cleanability using CIP Systems, simple validation.
Good product discharge characteristics with negligible product residues, due to narrow agitator to wall clearances, minimal vessel depth and a special agitator blade design.
Special properties for the customer's benefit
- Calculation, design and manufacture in compliance with Pressure Equipment Directive 97/23/EG or/and ASME U-Stamp as well as with cGMP and FDA guidelines
- EG type examination certification 03ATEX0246X in accord with PED 94/9/EG or with UL-approved electrical components for operations in class 1, division 1 or 2, group C & D environment
- Double mechanical seal, externally interchangeable, non-contacting gas-lubricated (lift-off), dry running contact (contacting sliding surfaces) or liquid-lubricated seal
- Sampler valve
- Pre-piping made of stainless steel on terminal box
- Excellent cleanability using CIP-systems, simple validation
Options
- Pressure-resistant and sterile versions, isolators (glove box), DQ, IQ, OQ qualification
- Autonomic PLC control or connected to PMSX, heavy current box