Sterile Manufacturing Vessel

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MOQ : 1 Piece

Sterile Manufacturing Vessel Specification

Temperature
Ambient to 121C (autoclavable)

Features
CIP/SIP system, Jacketed/Non Jacketed options, Agitator, Pressure Gauge, Temperature Sensor, Sterile Vent Filter, Sampling Valve

Noise Level
< 65 dB

Frequency
50/60 Hz

Phase
Single Phase/Three Phase

Usage & Applications
Sterile pharmaceutical manufacturing, biotech processing, sterile liquid and media preparation

Type
Sterile Manufacturing Vessel

Material
Stainless Steel (SS 316/SS 304)

Capacity
50 Liters to 20,000 Liters (customizable)

Computerized
Yes (optional as per requirement)

Control Mode
Automatic/Semi-Automatic

Voltage
220V/380V/415V (as per order specification)

Power
2 - 15 kW (depending on vessel size)

Weight (kg)
Varies as per capacity (approx. 250 kg - 2,500 kg)

Dimension (L*W*H)
Customized as per requirement

Color
Silver (Polished Stainless Steel)

Sterile Manufacturing Vessel Trade Information

Minimum Order Quantity
1 Piece

FOB Port
India

Payment Terms
Cash Advance (CA), Days after Acceptance (DA), Letter of Credit (L/C), Letter of Credit at Sight (Sight L/C), Cash Against Delivery (CAD), Telegraphic Transfer (T/T), Cash in Advance (CID), Cheque

Supply Ability
30 Pieces Per Week

Delivery Time
8 to 10 Months

Sample Available
Yes

Sample Policy
Contact us for information regarding our sample policy

Packaging Details
Wooden Packing Only

Main Export Market(s)
North America, South America, Eastern Europe, Western Europe, Middle East, Africa, Central America, Australia, Asia

Main Domestic Market
All India

Certifications
ISO and CE Certified

About Sterile Manufacturing Vessel

Salient Features:-

Design as per ASME code.
No stagnant point, internal surfaces are 0.28 Ra finish.
All contact parts/surfaces made out of SS 316/SS 316Lquality.
Electro polished from inside.
The vessel will be jacketed, insulated and cladded by SS 304sheet.
Spray ball for CIP/SIP system.
Flush bottom valve.
Steam/Electrical heating.
If required, Load cell/capacitance type level indicator will be provided to measure the volume inside the tank.

Superior Hygienic Design

With mirror-polished stainless steel surfaces and sanitary tri-clamp fittings, the vessel supports stringent cleaning and sterilization processes. This ensures product integrity and compliance with pharmaceutical and biotech standards.

Customizable Configurations

Users can select from a variety of options, such as mechanical or magnetic agitators, multiple gasket materials, pressure ratings, insulation, computerized controls, and electronic level indicators. Each vessel is built to exact specifications, suiting diverse sterile applications.

Comprehensive Documentation and Compliance

Each unit is delivered with full IQ/OQ/PQ documentation, supporting installation, qualification, and validation processes required in regulated industries. This streamlines facility audits and quality assurance.

FAQs of Sterile Manufacturing Vessel:

Q: How is the sterile manufacturing vessel cleaned and sterilized?

A: The vessel features Clean-in-Place (CIP) and Steam-in-Place (SIP) capabilities, allowing automated thorough cleaning and sterilization without dismantling, ensuring sanitary processing between batches.

Q: What applications are most suitable for this vessel?

A: This vessel is ideal for sterile pharmaceutical manufacturing, biotech processing, as well as preparation of sterile liquids and culture media, thanks to its hygienic design and customizable features.

Q: When should I choose insulation for the vessel?

A: Insulation is recommended when temperature-sensitive processes are involved or when energy efficiency is critical. Insulation is available on demand and can be tailored to specific process requirements.

Q: Where can the vessel be installed?

A: The vessel is suitable for installation in manufacturing plants, cleanrooms, and laboratories that require controlled, sterile environments for liquid processing and preparation.

Q: What does the documentation package include?

A: Each vessel is supplied with Installation Qualification (IQ), Operational Qualification (OQ), and Performance Qualification (PQ) documents, facilitating regulatory compliance and simplified validation.

Q: How do the safety features benefit my process?

A: Safety is enhanced with components like a pressure relief valve, emergency vent, and over-temperature alarm, minimizing operational risks and protecting personnel and product integrity.

Q: What are the benefits of choosing a customizable configuration?

A: Customizing your vessel ensures that it matches your process parameters, from capacity and control level to agitation type and utility connections, maximizing efficiency and process fit.

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