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COMPLIANCE & STANDARDS
COMPLIANCE & STANDARDS
AS 5369:2023 introduced significant changes to the reprocessing requirements for reusable medical devices within healthcare settings.
PodMed Supplies operates with systems and processes designed to work with these requirements.
Our Compliance Framework
Quality Systems
✓ ISO 9001 Audited & Certified
✓ Written policies and procedures
✓ Staff competency
✓ On going auditing
Sterilisation Controls
✓ Class 6 emulating indicators
✓ Printex process indicators
✓ Batch traceability systems
✓ Cycle validation and monitoring
Water Quality Management
✓ Reverse osmosis water systems
✓ Water quality testing
✓ Continuous monitoring of TDS, EC, pH and temperature
Facility & Workflow Controls
✓ Dirty to clean workflow separation
✓ Dedicated hand wash facilities
✓ Airflow and contamination considerations
Regulatory Compliance
✓ TGA Class I reusable instruments
✓ AS 5369:2023 compliant instruments
Full compliance documentation supplied with every sterilisation batch. This is email and uploaded onto your clinics portal.
Easy to use return tracking sheet included with every collection box.
Each order includes batch documentation with item tracking and compliance records.
QR code linked to batch records on your clinics portal
Batch tracking log included to support clinics traceability requirements.
Each sterile pack includes complete traceability labelling, including sterilisation date, batch number, expiry date, Printex process indicator label and QR code access to batch records via clinic portal
Lab test results for our reverse osmosis waster used for ultrasonic pre treatment, washing and final rinse
