Pharmaceutical Research Cabinet Isolator with PLC System in Cleanrooms

• Customization: Available
• Certification: GS, RoHS, CE, ISO9001
• Noise: Less Than 75
• Model NO.: M-ISLT-N
• Application: Industrial
• Control Mode: Touch
• Usage: Fragrance, Dust Removal, Smoke Removal, Adding Negative Ion, Humidification, Formaldehyde Formaldehyde, Adding Oxygen, Sterilization
• Inlet Air Speed: 0.45m/S±20%
• Rated Power: 4.2kw
• Indoor Illuminance: High Than 500 Lux
• Control Operation: PLC
• Illumination: More Than 300 Lux
• Airflow Mode: Turbulence
• Transport Package: Wooden Case
• Specification: 2400*2100*2450 mm
• Trademark: Miran
• Origin: China

Product Description

Pharmaceutical Research Cabinet Isolator with PLC System in Cleanrooms

Product Description

Negative pressure isolator M-ISOLATOR-N
It can meet the isolation operation of highly toxic, highly active, and highly allergenic drugs, comply with the requirements of EHS occupational health management system, and can be widely used in laboratories related to biomedicine, chemical engineering, and research institutes. Provide a sealed negative pressure environment for the packaging, weighing, ingredient preparation, sampling and other operational processes of drugs, to protect the health and safety of personnel throughout the entire operation process.

Product Parameters

Model	MCT-ISOLATOR-01
External dimensions	3000 ×850 ×2200 mm
Noise	≤75 dB
Illuminance	≥300 LUX
Airflow mode	turbulence
Operating cabin pressure	-100Pa ~ -20Pa
Power supply	AC220V,50Hz
Protection level	OEB 4
Cabin airtightness	Meet ISO10648-2 standard requirements
HEPA filter	PUSH-PUSHfilter

 

 

Detailed Photos

Advantages:

• SUS304 stainless steel production, customizable according to process requirements, negative pressure design;
• Provide flexible, high-quality, and high safety isolation and sealing operation plans for personnel, materials, environment, and equipment involved in the production process of highly toxic, highly active drugs, hormone drugs, and other API products. Provide environmental protection for sterile packaging, weighing, batching, crushing, sampling, etc;
• Optional water gun, air gun, etc. can be used to clean the cavity;
• C-RABS and ISOLATOR can be selected according to process requirements, and the biosafety leakage level can reach OEB-4
• RTP technology, AB valve group, or transfer window form can be designed for material entry and exit;
• Configurable bag in bag out.

Certifications

Production & Processing

 

Company Profile

 

Exhibitions

 

 

Packaging & Shipping

 

 

Why Choose Us?

• Well-experienced. Miran was founded in 2010.Focused on the pharmaceutical and chemical industry for over a decade
• Strong processing ability. We have independent research and development, production and manufacturing base, and more than 20 advanced processing equipment.
• Emphasis on R&D. We focuses on product research and innovation, with over ten R&D personnel and more than thirty patent certificates
• Complete verification.The verification system is complete, with a dedicated verification team responsible, complete verification materials, and a comprehensive after-sales service system
• Professional.Focusing on the pharmaceutical industry, familiar with pharmaceutical production processes, understanding and deepening the concept of verification system,

FAQ:
Q1: Are you a manufacturer?
Ans: *1.Yes, we have been in manufacturing and providing excellent cleanroom and solid preparation front-end processing system for customers more than 10 years.
*2.Our own production plants and a wide network of suppliers who are strictly selected, are totally qualified for ISO Quality Management System. 
Q2: Do you inspect the finished products? 
Ans:Yes, we will do inspection according to ISO standard and ruled by our QC staff. 
Q3: Do you do OEM or ODM?
A:Yes, we do OEM and ODM. Customer's LOGO can be printed on our products
Q4: How long is the delivery time?
Ans: Normally 7days if we have the sample on hand. If customized one, about 60days.
Q5: How long is the warranty period?
 Ans: One year after shipment.