Medical Device Package Integrity Test

EUROLAB performs dye penetration and microbial stress pack integrity tests. Package integrity tests are used to detect packaging issues that can adversely affect the sterility of a medical device.

Sterile products can be subjected to an environmental stress that aims to simulate the extreme conditions a product may encounter in shipping or storage. The product packaging is then subjected to microbial strain or dye penetration testing to determine whether it retains its properties as a microbial barrier.

Package Integrity Tests

Package Integrity with Microbial Challenge (26 samples recommended)
Package Integrity According to Dye Penetration (13 samples are recommended)
Bursting Strength Test
Seal Shell

Medical Tests

Medical Device Package Integrity Test
IEC 60601-1 Medical Electrical Equipment Test
EMC Tests for Medical Devices
Hospital Sterilization Water Analysis
IEC 62133 Battery Safety Test for Medical Devices
Medical Device Biocompatibility Test
Biocompatibility Test
Biological Safety Analysis
Chemical Characterization Analysis
Medical Device Cleaning Analysis
Long Accelerated Shelf Life Test
Packaging Verification and Shelf Life Test
Particle Analysis
Medical Device Sterilization Verification Tests
Microbiological Testing Services
Medical Device Biocompatibility Test - ISO 10993
Bacterial Endotoxin and Pyrogen Test
USP 88 Plastic Tests
Medical Device Chemical Characterization ISO 10993-18
Latex Antigenic Protein Test
Medical Device Shelf Life / Aging Test
Implantable Medical Device Test
Antibiotic Potency Test
Medical Device Product and Packaging Tests
EN/IEC 62366 Usability Engineering Tests for Medical Devices
Disinfectant Testing Services
ISO 10993-11 Biological Evaluation of Medical Devices - Part 11: Systemic Toxicity Tests
ISO 10993-17 Biological Evaluation of Medical Devices - Part 17: Determination of Acceptable Limits for Leachable Substances
ISO 10993-18 Biological Evaluation of Medical Devices - Part 18: Determination of Chemical Properties of Medical Device Materials in a Risk Management Process
Medical Device Disinfection Verification
Medical Device Efficiency Test
ISO 22196 - Testing for Modified Antimicrobial Surfaces for Viruses
Microbial Access Test
Needle Free Connector Microbial Access Test
Wound Dressing Microbial Access Test
Antimicrobial Efficacy Test of Treated Dressings
CDC Duodenoscope Surveillance Sampling
Dioxin Analysis
Biocidal Analysis
Load Frame Test
Pin-on-Disc (POD) Test
Hip Simulator Wear Test
Knee Simulator Wear Test
Biomechanical Testing
Hip Device Test
Knee Device Test
Shoulder Device Test
Ankle Device Test
Spine Device Test
Osteosynthesis Device Test
Material and Coating Test
Stent and Stent Graft Test
Vascular Graft Test
Catheter Test
Heart Valve Test
Coating Integrity and Acute Particle Test
MRI Compatibility and Safety Testing
Acute Systemic Toxicity Test
Absorption Capacity Test
Distribution Cycle Test
MDR Medical Device Testing
Oxygen Compatibility Test
Product Inoculation Test
Clinical Party Release Test
D-Value Determination Test
Bioburden Test
Microbial Definition Test
Viral Penetration Test
Hemocompatibility Tests
Reusable Medical Devices Tests
Medical RFID Test
Orthopedic Device Tests
Cardiovascular Device Tests

Medical Tests

Medical Device Package Integrity Test

Package Integrity Tests

Medical Tests

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