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ISO 5 Modular Dust Free Room With GMP Standard CE Certificates

Productgegevens

Plaats van herkomst: CHINA

Merknaam: ZJNF

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Min. bestelaantal: 1

Prijs: negotiate

Verpakking Details: multiplex/houten pakket

Levertijd: 18 dagen

Betalingscondities: TT LC PayPal -creditcard

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Specificaties
Markeren:

ISO 5 modular clean room

,

GMP standard dust free room

,

CE certified modular clean room

Sollicitatie:
100 Lab / Laboratorium Clean Room, Farmaceutisch, Chemisch lab, elektronische fabriek, ziekenhuis
Luchtwisseling:
100.000-grade 10-15 keer/uur
Type:
Clean Room Booth, modulaire ontwerpen, cleanroom
Intelligente milieucontrole:
10-inch touchscreen Integrated Control System biedt realtime monitoring van temperatuur, vochtigheid
Lichaamsmateriaal:
Koud-roll staal / roestvrij staal
Productcategorie:
Modulaire schone kamer
Modulair structureel ontwerp:
Hoofdraamwerk, envelopsystemen en zuiveringsapparatuur (FFUS/luchtdouches, enz.) Zijn geprefabriceer
Nieuwe energie/R&D:
Snelle inzetoplossingen voor EV-batterijworkshops en universitaire laboratoria, ideaal voor kleinsch
Sollicitatie:
100 Lab / Laboratorium Clean Room, Farmaceutisch, Chemisch lab, elektronische fabriek, ziekenhuis
Luchtwisseling:
100.000-grade 10-15 keer/uur
Type:
Clean Room Booth, modulaire ontwerpen, cleanroom
Intelligente milieucontrole:
10-inch touchscreen Integrated Control System biedt realtime monitoring van temperatuur, vochtigheid
Lichaamsmateriaal:
Koud-roll staal / roestvrij staal
Productcategorie:
Modulaire schone kamer
Modulair structureel ontwerp:
Hoofdraamwerk, envelopsystemen en zuiveringsapparatuur (FFUS/luchtdouches, enz.) Zijn geprefabriceer
Nieuwe energie/R&D:
Snelle inzetoplossingen voor EV-batterijworkshops en universitaire laboratoria, ideaal voor kleinsch
Beschrijving
ISO 5 Modular Dust Free Room With GMP Standard CE Certificates

Modular cleanrooms, as the core solution for modern industrial clean environments, demonstrate their key value in two dimensions: rapid deployment and flexible adaptability.

Through standardized prefabricated components manufactured in factories and assembled on-site, the construction period can be reduced to 1/10 of that of traditional cleanrooms (typically requiring only 3-5 days).

They also support module reconfiguration during production line expansion or process adjustments, with material reuse rates as high as 98%.

This structure is particularly suitable for industries with high cleanliness requirements and frequent production line iterations, such as electronics manufacturing and biopharmaceuticals.

In scenarios like semiconductor packaging and sterile drug production, modular cleanrooms not only meet the cleanliness level requirements of ISO 14644-1 standards but also enable real-time monitoring and control of parameters such as temperature, humidity, and pressure differentials through intelligent monitoring systems, forming a clean environment system that combines timeliness and functionality.

In terms of cleanliness control, modular cleanrooms achieve precise classification through a three-stage filtration system: first, the primary filter in the FFU (Fan Filter Unit) intercepts particles ≥5μm; then, HEPA/ULPA high-efficiency filters (with ≥99.97% filtration efficiency for particles ≥0.3μm) perform core purification; finally, a laminar airflow system maintains unidirectional airflow.

This design can stably achieve cleanliness levels from ISO Class 5 (Class 100) to ISO Class 8 (Class 10,000). For semiconductor-grade applications, which typically require ISO Class 3 (Class 10) environments, ULPA filters (with ≥99.9995% filtration efficiency for particles ≥0.12μm) and vertical laminar airflow organization are necessary.

Notably, cleanliness levels and energy consumption exhibit an exponential relationship—Class 100 cleanrooms require 300-600 air changes per hour, while Class 10,000 only needs 20-60.

Therefore, modular designs incorporate zoning control functions, allowing independent operation of areas with different cleanliness levels, significantly reducing overall energy consumption.

In practical applications, biosafety laboratories often adopt a combination of ISO Class 5 core areas and ISO Class 7 buffer zones, ensuring operational safety while avoiding energy waste.

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