Pharmaceutical Crusher CGMP

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Pharmaceutical Crusher CGMP Specification

Type
Pharmaceutical Crusher CGMP

Material
Stainless Steel

Capacity
10-50 kg/hr

Computerized
No

Automatic Grade
Semi-Automatic

Voltage
220 V

Frequency (MHz)
50 Hz

Size
Medium

Weight
Approx. 120 kg

Dimension (L*W*H)
750 mm x 500 mm x 1200 mm

Noise Level
Low

Discharge Type
Bottom Discharge with Sieve

Application
Pharmaceutical, Laboratory

Blade Material
Hardened Stainless Steel

Safety Features
Interlock and Overload Safety

Finish
Mirror/Matte

Mobility
Mounted on CASTOR wheels

Crushing Chamber
Easy to clean, GMP model

About Pharmaceutical Crusher CGMP

Specification

Type Of Crushing Machines	PRE CRUSHER
Capacity	15KG UPTO 2 TON
Brand	Shubh
Model Name/Number	SHUBH GRINDER PRE CRUSHER
Material	MS/SS/CGMP
Automation Grade	Automatic
Motor Power	1 HP upto 30 HP
Model	SHUBH GRINDER PRE CRUSHER
Chamber Size	4" TO 24"
Material Grade	SS 304/ SS316

Engineered for Pharmaceutical Precision

The Pharmaceutical Crusher CGMP is tailored to meet stringent industry standards. Designed for medium capacity operations, its hardened stainless steel blade efficiently crushes pharmaceutical substances while maintaining product integrity. The easy-to-clean chamber and sanitary mirror/matte finish align with GMP requirements, supporting both laboratory and industrial use cases.

Mobility and Convenience Combined

Thanks to its sturdy castor wheels, this crusher can be moved effortlessly between workstations. Its thoughtful bottom discharge system with a sieve assures consistent particle size while making product collection straightforward and spill-free. These features, alongside its semi-automatic operation, optimize workflow in busy pharmaceutical environments.

FAQ's of Pharmaceutical Crusher CGMP:

Q: How is the Pharmaceutical Crusher CGMP cleaned after use?

A: The design features an easy-to-clean crushing chamber that allows for swift sanitation. Components made from stainless steel and a smooth mirror/matte finish reduce the risk of contamination and facilitate thorough cleaning between batches, crucial for GMP compliance.

Q: What materials can the crusher process, and what is its typical application?

A: This crusher is engineered for pharmaceutical and laboratory settings, effectively processing a range of solid pharmaceutical ingredients. It is suitable for crushing tablets, granules, or raw materials before further processing or formulation.

Q: When should the interlock and overload safety features be used?

A: These safety mechanisms function automatically. The interlock prevents operation when access panels are open, ensuring operator safety, while the overload protection stops the machine if excessive load is detected, preventing mechanical damage and ensuring consistent performance.

Q: Where is the crushed product collected after processing?

A: Crushed materials exit through the bottom discharge, which is fitted with a sieve. This setup efficiently collects the finished product and ensures only suitably sized particles pass through, ready for subsequent pharmaceutical processes.

Q: What is the process for operating the Pharmaceutical Crusher CGMP?

A: Operation involves loading materials into the chamber, ensuring the safety interlock is engaged, and selecting the desired discharge sieve size. The semi-automatic system manages the crushing cycle, and finished product is simply collected from the bottom discharge port.

Q: What benefits does the hardened stainless steel blade provide?

A: The blade's hardened stainless steel composition offers superior durability, resistance to corrosion, and maintains sharpness during repetitive use. This ensures reliable, consistent crushing performance and long operational life, tailored to pharmaceutical industry demands.

Q: How does the Pharmaceutical Crusher CGMP support GMP compliance?

A: The model features easy-to-clean surfaces, a sanitary finish, interlocks for operator safety, and bottom discharge for minimal contamination. These design elements align with GMP requirements, ensuring hygienic operation and regulatory compliance in pharmaceutical production.

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