Medische apparatuur

Medische apparatuur

Precision Cleanroom Environments for Medical Device Manufacturing

Uitdagingen in de industrie:

ISO 13485 Compliance: Stringent environmental control for assembly and sterile packaging.
Process Versatility: Different zones require different ISO classes (e.g., ISO 7 for assembly, ISO 8 for packaging).

De oplossing van UPTING:

We provide flexible, modular cleanrooms that allow for easy zoning. Our pre-engineered systems ensure rapid setup of sterile testing labs and high-grade assembly lines.

Uitgelichte projecten:

Nanwei Medical: Built a comprehensive 25,000 m² cleanroom manufacturing facility and laboratory in Thailand for the leading endoscopic device manufacturer.

FAQs about Medical Equipment Cleanrooms

Q: Can you design a facility with different ISO classes in different zones?

A: Yes. We specialize in designing dynamic cleanroom layouts with tailored pressure cascades and airlock systems, allowing you to seamlessly connect an ISO 7 assembly zone with an ISO 8 packaging area.

Q: Can we expand or modify the cleanroom later if we add new product lines?

A: That is the primary advantage of our modular "Clean Cube" system. The pre-engineered panels and grids can be easily disassembled, reconfigured, or expanded with minimal waste and downtime.

Q: Do you manufacture the purification equipment used in these rooms?

A: Yes, UPTING is a true source manufacturer. We produce the FFUs, HEPA filters, air showers, and pass boxes in-house, ensuring perfect integration, strict quality control, and competitive pricing.

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