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7500m3/H ISO Class 8 Clean Room Dust Free , 220V 63dB Medical Device Cleanroom

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7500m3/H ISO Class 8 Clean Room Dust Free , 220V 63dB Medical Device Cleanroom

Name: 7500m3H ISO Class 8 Clean Room Dust Free 220V 63dB Medical Device Cleanroom
Brand: anlaitech
Price: 1 USD

China 7500m3/H ISO Class 8 Clean Room Dust Free , 220V 63dB Medical Device Cleanroom wholesale

Brand Name : anlaitech

Model Number : AL-MODULAR CLEAN ROOM

Certification : CE , FAT, CLASS REPORT

Place of Origin : CHINA

MOQ : 1set of china clean room

Payment Terms : L/C, T/T, Western Union

Delivery Time : 12WORKING DAYS.

Packaging Details : standard exporting packing for clean room china

Name : 7500m3/H ISO Class 8 Clean Room Dust Free , 220V 63dB Medical Device Cleanroom

Material : Sandwich panel stainless steel /Painted steel+plexiglass

Product Name : clean room, lab clean room, modular clean room, cleanroom

Application : lab clean room, optics clean room, electronical clean room,Pharmaceutical clean room..etc

Power supply : 220V/50Hz

Air flow (m3/h) : 7500m3/H

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ISO Class 8 Dust free Medical Device Cleanroom workshop and manufacturer

Medical Device Cleanroom sulotions:

(1) It is crucial to maintain a contaminant-free clean environment when manufacturing medical devices such as biological implants. This starts with the cleanroom design and management systems. The cleanroom design prevents outside contamination, while regular maintenance and sanitation upkeep minimize the risk of contamination originating within the cleanroom itself.

(2) Implants that are non-sterile or are awaiting sterilization should be subject to purification and clean packaging processes. This will allow for uniformity and control over product quality. When constructing a GMP Medical Instrument Cleanroom, a location should be designated for the packaging process, and processes should be implemented to ensure that products avoid contamination risk at all times.

(3) Procedures must be developed to control environments in which there exists a contamination risk to products. This includes any time personnel makes contact with a product, including when products are moved from one location to another.

Maximum Particles/m³
≥0.1μm	≥0.2μm	≥0.3μm	≥0.5μm	≥1μm	≥5μm
ISO 3	1,000	237	102	35b	d	CLASS 1
ISO 4	10,000	2370	1,020	352	83b	CLASS 10
ISO 5	100,000	23700	10,200	3,520	832	CLASS 100
ISO 6	1,000,000	237,000	102,000	35,200	8,320	CLASS 1000

Application: E-Cigarette, LCM, CMOS Camera Module, Touch Play, Optical Module, FILM, Biological Pharmacy,

Packing,Food

Main Features
(1) Assembly structure designed, easy installation and easily moved
(2) Directional wheels can be installed, suitable for small building and high cleanliness area;
(3) Modular design: clean booth can be as small as several square meters and can be as large as hundreds of square meters
(4) It has large useful and effective area; while compared with traditional clean room, it has such features like low investment, high return and stable.

7500m3/H ISO Class 8 Clean Room Dust Free , 220V 63dB Medical Device Cleanroom

Specification

Model item		ISO 8 CLEAN ROOM
Model item		AL-CS4*6/C8	AL-CS5*10/C8	AL-CS6*12/C8	AL-CS7*20/C8
Size(mm)		400060002500	5000100002500	6000120002500	7000200002500
Material	Framework	Cold rolled steel /Aluminum/Stainless steel/sandwich panel
Material	Around	Plexiglass,Soft curtain,Anti-static strip curtain/sandwich panel
Clean Class Level		10000	10000	10000	10000
HEPA filter	Size(mm)	61061069	122061069	122061069	122061069
	Efficiency(%)	99.99	99.99	99.99	99.99
	Air flow (m3/h)	3600	7500	10800	21000
Pre filter	Size(mm)	Optional
Motor Spec	Power supply	220V/50Hz	220V/50Hz	220V/50Hz	220V/50Hz
Motor Spec	Noise(dB)	62	63	62	63

What We Can Do For You?

Front end consultancy support, Concept design and engineering.

Clean room design and construction.

Unique range of clean room modular walls and ceilings, flooring system.

Cleanroom accessories (pass boxes, step over benches, change room furniture and fittings, sampling and dispensing booths, air showers, etc.) GRP clean room doors.

Equipment selection ,Validation master plans, protocols and continuous monitoring systems regulatory advise.

HVAC Design and Installation.

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