Noncritical, noninvasive devices that can be reprocessed

Arjo ReNu's™ quality assurance processes comply with GMP’s and 21CFR820 regulations, and include:

  • Unique bar code identifiers applied to individual devices to track each step of their functional life and provide complete traceability
  • Tracking and monitoring of every HLD production number, including time and temperature, to ensure that 100% of devices achieve high-level disinfection
Compression garments Lateral transfer matts ECG leads Pulse oximeters
Slings Pneumatic tourniquets Infusor bags

If you would like more information about Arjo ReNu, please contact us.

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