Why Test Medical Devices?
Medical devices directly impact patient safety. Even the smallest failure in material, cleanliness, or sterility can cause harm, trigger recalls, and destroy brand trust.
Testing ensures:
- Devices are safe, effective, and reliable
- Compliance with ISO 13485, FDA, EU MDR, BIS, and CDSCO
- Smoother approvals and market entry
- Reduced risk of recalls and penalties
Types of Medical Device Testing We Provide
Biocompatibility Testing
Why: To ensure device materials are safe for human use.
What we test: Cytotoxicity, irritation, sensitization, hemocompatibility, systemic toxicity.
Who needs it: Implantable and non-implantable device manufacturers.
Cleaning Validation
Why: Residual contaminants can cause infections or device failure.
What we test: Residual protein, endotoxins, detergents, microbial residues.
Who needs it: Reusable medical devices, surgical instruments, endoscopes.
Sterility & Microbial Testing
Why: Devices must remain sterile until point of use.
What we test: Sterility assurance, bacterial endotoxins, bioburden testing.
Who needs it: Single-use devices, sterile packaging, surgical kits.
Physical & Mechanical Testing
Why: Devices must perform as intended under stress and usage.
What we test: Tensile strength, durability, functionality, packaging integrity.
Who needs it: Consumables, implants, surgical tools, diagnostic devices.
Chemical Characterization
Why: To identify harmful chemicals that may migrate from device materials.
What we test: Volatile/semivolatile organics, heavy metals, residual solvents.
Who needs it: Plastic, polymer, and coated medical devices.
Benefits of Testing with Prewel Labs
Compliance Simplified
Meet ISO 10993, ISO 13485, FDA, EU MDR, BIS, and CDSCO requirements.
Digital Dashboard
Real-time results, audit-ready reports, and AI foresight.
Risk Prevention
Detect issues early before they reach patients.
Global Readiness
Testing aligned with international regulatory expectations.
Brand Protection
Demonstrate safety and earn trust with regulators & clinicians.
Who We Serve
Medical Device Manufacturers
Implants, surgical instruments, consumables
Diagnostic Companies
Devices, kits, and testing consumables
Hospitals & Healthcare Providers
Cleaning validation for reusable instruments
Exporters & Global Med-Tech Firms
Compliance for FDA, EU MDR, and WHO markets
Medical Device Testing at a Glance
| Test Type | Why It Matters | Key Parameters | Who Needs It |
|---|---|---|---|
| Biocompatibility | Ensures device material safety | Cytotoxicity, sensitization, hemocompatibility | Implant & non-implant device makers |
| Cleaning Validation | Prevents infections, ensures safe reuse | Residual protein, endotoxins, microbial residues | Hospitals, reusable device makers |
| Sterility & Microbial | Maintains sterility & patient safety | Sterility assurance, endotoxins, bioburden | Single-use device manufacturers |
| Physical & Mechanical | Confirms performance & durability | Tensile strength, packaging integrity | Implants, surgical tools, consumables |
| Chemical Characterization | Detects harmful extractables/leachables | Organics, metals, solvents | Polymer/plastic-based devices |