Pharmaceutical Filtration Unit
Pharmaceutical Filtration Unit

Pharmaceutical Filtration Unit

Pharmaceutical Filtration Unit Specification

  • Temperature
  • Up to 80C
  • Phase
  • Single / Three Phase
  • Noise Level
  • <60 dB
  • Usage & Applications
  • Pharmaceutical liquid filtration, sterile filtration, water purification
  • Features
  • Corrosion resistant, High filtration efficiency, Easy to clean, Sanitary design
  • Frequency
  • 50 Hz
  • Type
  • Filtration Unit
  • Material
  • Stainless Steel (SS 316L)
  • Capacity
  • 50 to 500 Liters per Hour
  • Computerized
  • No
  • Control Mode
  • Manual / Semi-automatic
  • Voltage
  • 220V / 380V
  • Power
  • 1.5 kW
  • Weight (kg)
  • 120 kg
  • Dimension (L*W*H)
  • 1150 mm x 510 mm x 1200 mm
  • Color
  • Silver
  • Filtration Accuracy
  • 0.2 - 1 micron
  • Mounting
  • Castor wheel mobile
  • Pump Type
  • Centrifugal sanitary pump
  • Inlet/Outlet Size
  • 1.5 inch TC connection
  • Serviceability
  • Tool-free quick disassembly
  • Compliance
  • GMP, FDA approved design
  • Maximum Working Pressure
  • 4 bar
  • Filter Element Material
  • Polypropylene / PTFE
  • Cleaning
  • CIP/SIP compatible
  • Operation Environment
  • Indoor cleanroom
 

Pharmaceutical Filtration Unit Trade Information

  • FOB Port
  • yes
  • Payment Terms
  • Cash on Delivery (COD), Letter of Credit (L/C), Telegraphic Transfer (T/T), Western Union, Paypal, Cash Against Delivery (CAD), Cash in Advance (CID), Cheque, Cash Advance (CA)
  • Supply Ability
  • 100 Per Year
  • Delivery Time
  • 3 Week
  • Sample Policy
  • Free samples available with shipping and taxes paid by the buyer
  • Packaging Details
  • PACKING, WOODEN BOX
  • Main Export Market(s)
  • Australia, North America, Eastern Europe, Western Europe, Middle East, South America, Asia, Central America, Africa
  • Main Domestic Market
  • All India
  • Certifications
  • ISO 9001 : 2015
 

About Pharmaceutical Filtration Unit

Microtech engineering offer offer candle perfume filter press with candle cleaning system electrical flameproof.

Technical Specifications:

Model

No. Of candles

4 nos

6 nos

Filtering candles

S. S. 316 / 10-20 micron

S. S. 316 / 10-20 micron

Output(ltrs/hr)

800-1500 ltrs/ hr/

2000-3000 ltrs/ hr/

Liquid holding

a0a after full transfer

a0a after full transfer

Thickness of shell

3mm thick

3mm thick

Thick of top- bottom cover

5 mm thick

5 mm thick

Length of candle

200 mm

200 mm

Inlet conical filter

6a dia x s. S. Mash

6a dia x s. S. Mash

Process inlet outlet

1a dia hose nipple

1 A12 a dia hose nipple

Direct use pump connection

1a bsp ball valve / 1 A12 a hose nipple.

1 A12 a bsp ball valve / 1 A12 a hose nipple.

Candle cleaning system

1 candle clean at a time

1 candle clean at a time

Pump mechanical seal

s. S. 316 Teflon.

s. S. 316 Teflon.

Pump motor

2hp / 440 rpm / 3 ph / flame-proof

3 hp / 440 rpm / 3 ph / flame-proof

Air vent- safety valve

A14 BSP.

A14 BSP.

Drain valve

1a BSP

1a BSP

M. O. C

s. S. 304 l / 316

s. S. 304 l / 316

Finish

Polished to mirror finish.

Polished to mirror finish.


Salient Features:
  • All contact parts made out of s. S. 304 l material.No requirements of any filter pad / filter.
  • S. S. Candle for crystal clear filtration & long lasting.
  • Option: - pump can be use separately for water transfer or usually with the filter press.
  • a0a (zero) holding.
  • Outer & inner mirror finish buffing for easy cleansing.
  • Easy opening, fitting & cleansing.


Precision Filtration for Pharmaceutical Liquids

Designed to deliver reliable sterile filtration, this unit achieves accuracy down to 0.2 microns, making it suitable for removal of bacteria and particulates from pharmaceutical liquids and water. Its sanitary design, mobile mount, and easy-to-clean features ensure hassle-free operation in indoor cleanroom environments.


Robust Construction and Compliance

Built from SS 316L stainless steel for corrosion resistance, the filtration unit is compliant with both GMP and FDA standards. It supports tool-free disassembly for fast servicing and integrates seamlessly with Clean-In-Place (CIP) and Steam-In-Place (SIP) cleaning protocols for optimal hygiene.

FAQ's of Pharmaceutical Filtration Unit:


Q: How is the Pharmaceutical Filtration Unit cleaned and maintained?

A: The unit is compatible with Clean-In-Place (CIP) and Steam-In-Place (SIP) protocols, allowing for thorough internal cleaning without disassembly. Additionally, its tool-free quick disassembly feature enables easy access for maintenance so cleaning and servicing are straightforward and efficient.

Q: What types of liquids can be processed with this filtration unit?

A: This unit is suitable for filtering pharmaceutical liquids, supporting sterile filtration and water purification. The filtration accuracy of 0.2 - 1 micron efficiently removes particulate contamination, making it ideal for environments where ultra-clean filtered liquids are required.

Q: When is it recommended to use this filtration unit in the pharmaceutical process?

A: Use this unit during critical steps that require sterile filtration, such as before formulation, filling, or packaging. It is designed for operations in indoor cleanroom environments where contamination control is essential, ensuring product safety and compliance.

Q: Where should the Pharmaceutical Filtration Unit be installed for optimal performance?

A: It is intended for use in indoor cleanroom settings, where conditions meet GMP and FDA compliance. Its mobile castor wheel base allows flexible positioning, enabling seamless integration into various pharmaceutical production and purification workflows.

Q: What is the process for changing filter elements in the unit?

A: Filter elements made of polypropylene or PTFE can be changed quickly thanks to the tool-free disassembly design. Operators simply unlock the filter housing, replace the element, and restore operation-requiring no special equipment or extended downtime.

Q: Why choose this filtration unit for pharmaceutical applications?

A: Its high filtration efficiency, corrosion-resistant construction, compliance with international standards, and ease of cleaning make it ideal for stringent environments. By ensuring consistent performance and purity, it safeguards product quality and supports regulatory requirements.

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