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  1. Industries
  2. Medical Devices Services

Medical Devices Laboratory Services

Medical Devices

ContractLaboratory.com can assist your medical device  manufacturer, organization, academic institution, or government agency in outsourcing independent, commercial contract laboratories and contract research organizations (CRO) to do all your routine and non-routine Medical Devices and In-Vitro Diagnostics testing, medical device analysis, medical device certification, medical device experiments and medical device research and medical device development studies. Medical Devices, In-Vitro Diagnostics, biomedical, biophysical, bio mechanical studies, research, development, experimentation, evaluations, analysis, and testing. Some medical device certification 

 


Medical Devices Testing and Research Services

Contract Laboratory can help you with all your Medical Devices testing, analysis, scientific research and development, inspection, certification, engineering, failure investigation, and product development needs including:

  • Biomaterials
  • of Tissues
  • Bone and Joint Computer Modeling
  • Ethylene Oxide Biological Indicators Performance
  • GHG Emissions
  • Implantable Medical Device
  • In-Vitro Diagnostic
  • Precision
  • Sensitivity
  • Specificity
  • Medical Device AATCC and ASTM Antimicrobial
  • Medical Device ASTM Extractable
  • Medical Device Barrier
  • Medical Device Bioburden
  • Total Aerobes
  • Total Coliforms
  • Total Fungi
  • Medical Device Biodegradation Subchronic Toxicity Studies
  • Medical Device Biomaterial Extracts Protein Assays
  • Medical Device Carcinogenicity
  • Medical Device Compliance
  • Medical Device Container/Closure
  • Medical Device Contamination
  • Medical Device Design and Modeling of Systems Medical Device Environmental Monitoring
  • Medical Device Ex-Vivo Hemocompatibility Studies Medical Device Finished Product Quality Control
  • Medical Device Genotoxicity Ames
  • Medical Device Genotoxicity Chromosomal Aberration
  • Medical Device Histopathology
  • Medical Device ISO 10993-1 (FDA GP 95-1) Biological Safety
  • Medical Device In-Vitro Biocompatibility Studies
  • Medical Device In-Vivo Biocompatibility Studies Medical Device In-Vivo Hemocompatibility Studies
  • Medical Device Irritation Studies
  • Medical Device Leachable
  • Medical Device Microbial Identifications
  • Medical Device Mutagenicity
  • Medical Device Particles Analysis
  • Medical Device Particulate
  • Medical Device Physical
  • Medical Device Preclinical
  • Medical Device Product Inoculations
  • Medical Device Product Safety
  • Medical Device Radiological
  • Medical Device Sensitization
  • Medical Device Shipping Validations and Shipping
  • Medical Devices Impact Resistance
  • Simulated Use
  • Medical Device Stability Studies
  • Medical Devices Accelerated Aging Stability Studies Medical Devices Real Time Stability Studies Medical Device Sterility
  • Medical Device Sterilization Dose Validation Medical Device Sterilization Validation Medical Device Tensile
  • Medical Device Thermal Analysis
  • Medical Device USP Implantation Studies Medical Device USP Microbial Limits
  • Medical Device USP and EP Plastics and Container
  • Medical Device USP Glass Container
  • Medical Device USP Polyethylene Container
  • Medical Device USP
  • AAMI
  • EP Bacteriostasis/Fungistasis
  • Medical Devices Analytical Chemistry
  • Medical Devices Bacterial Endotoxin
  • - Gel Clot
  • Medical Devices Bacterial Endotoxin
  • - Limulus Amebocyte Lysate LAL
  • Medical Devices Biomaterials
  • Medical Devices Biomechanical Platform
  • Medical Devices Biomechanical
  • Medical Devices Biomedical
  • Medical Devices Biomedical
  • Medical Devices Biophysical Characterization
  • Medical Devices Biophysical Properties
  • Medical Devices Biophysical
  • Medical Devices Cleaning Validation
  • Medical Devices Conformity Assessments
  • Medical Devices Cytotoxicity
  • Medical Devices Electrical Safety
  • Medical Devices Electromagnetic Compatibility
  • EMC
  • Medical Devices Ethylene Oxide Residuals
  • Medical Devices Failure Analysis
  • Medical Devices Fatigue
  • Medical Devices Fatigue
  • Medical Devices Foreign Materials
  • Medical Devices In-Vivo USP
  • JP
  • EP Pyrogen
  • Medical Devices Leak
  • Medical Devices Materials Characterization
  • Medical Devices Methods Development and Validation
  • Medical Devices Microbiology
  • Medical Devices Packaging Studies and
  • Medical Device Package Integrity
  • Medical Device Packaging Burst
  • Medical Device Packaging Creep
  • Medical Device Packaging Dye Penetration
  • Medical Device Packaging Peel
  • Medical Device Packaging Vacuum Leak
  • Medical Devices Safety Evaluations
  • Medical Devices Toxicology
  • Medical Devices Transportation Simulation
  • Medical Devices Vibration
  • Medical Products Re-engineering
  • Medical Products Reverse Engineering
  • Reusable Device Studies
  • Reusable Medical Devices
  • RoHS
  • Steam Biological Indicators Performance
  • USP Purified Water
  • USP Water for Injection
  • WEEE

Type of Medical Devices Products

Contract Laboratory can assist your company, academic institution, government agency or organization in outsourcing contract laboratories to perform testing, analysis, and product development for many Medical Devices finished products, processes, systems, in-process materials, raw materials and components such as:

  • pediatric medical devices
  • in-vitro diagnostic devices
  • sterile implantable medical devices
  • orthopedics
  • pacemakers
  • stents
  • artificial hearts
  • knee replacements
  • hip replacements
  • physical medicine devices
  • radiology devices
  • nuclear medicine devices
  • NMR
  • CAT scanning machines
  • PET scanning machines
  • disposable medical devices
  • contact lenses
  • hearing aids
  • cochlear implants
  • blood glucose meters
  • pregnancy test kits
  • latex gloves
  • breast implants
  • surgical gloves
  • condoms
  • intraocular lenses
  • glasses
  • IV
  • needles
  • blood bags
  • reproductive devices
  • nebulizers
  • mammography machines
  • single-use medical devices
  • electrical medical devices
  • biological medical devices
  • X-Ray Systems
  • wireless medical telemetry
  • lasers
  • anesthesiology medical devices
  • surgical devices
  • sutures
  • angioplaty devices
  • apnea monitors
  • catheters
  • defibrillators
  • aneurysm clips
  • dressings
  • cardiovascular medical devices
  • ear
  • nose and throat medical devices
  • orthopedic medical devices
  • microbiology medical devices
  • opthalmic medical devices
  • pathology medical devices
  • toxicology medical devices
  • dental medical devices
  • immunology medical devices
  • neurology medical devices
  • surgery medical devices
  • plastic medical devices
  • medical gases
  • reusable medical devices
  • hospital beds
  • wheelchairs


Medical Devices Test Methods and Standards

Contract Laboratory can help with testing, analysis, assays, evaluations, examinations, inspections and certifications to different Medical Devices test methods, standards, procedures or specifications.

  • ASTM 27186:2010 - Active implantable medical devices - Four-pole connector system for implantable cardiac rhythm management devices - Dimensional and test requirements.
  • ANSI 14117:2012 - Active implantable medical devices - Electromagnetic compatibility - EMC test protocols for implantable cardiac pacemakers
  • AAMI TIR42:2010 - Evaluation of particulates associated with vascular medical devices
  • ANSI 80369-20:2015 - Small-bore connectors for liquids and gases in healthcare applications - Part 20: Common test methods.
  • ANSI 16142-2:2017 - Medical devices - Recognized essential principles of safety and performance of medical devices - Part 2: General essential principles and additional specific essential principles for all IVD medical devices and guidance on the selection of standards
  • ISO - Cardiovascular biological evaluation of medical devices - Guidance for absorbable implants.
  • ISO 10993-20:2006 - Biological evaluation of medical devices - Part 20: Principles and methods for immunotoxicology testing of medical devices
  • ANSI TIR10993-19:2006 - Biological evaluation of medical devices - Part 19: Physio-chemical
  • ANSI 10993-6:2016 - Biological evaluation of medical devices Part 6: Tests for local effects after implantation
  • ANSI 10993-5:2009/(R)2014 - Biological evaluation of medical devices - Part 5: Tests for in vitro cytotoxicity.
  • ANSI 10993-3:2014 - Biological evaluation of medical devices-Part 3: Tests for genotoxicity
  • ANSI 10993-14:2001/(R)2011 - Biological evaluation of medical devices
  • ANSI 10993-13-2010/(R)2014 - Biological evaluation of medical devices
  • ANSI 10993-10:2010/(R)2014 - Biological evaluation of medical devices - Part 10: Tests for irritation and skin sensitization.
  • ISO 11.040.01 - Medical equipment in general
  • IEC 80601-2-35:2009 - Medical electrical equipment -- Part 2-35: Particular requirements for the basic safety and essential performance of heating devices using blankets
  • IEC 60601-2-52:2009 - Medical electrical equipment -- Part 2-52: Particular requirements for the basic safety and essential performance of medical beds
  • ISO 22882:2016 - Castors and wheels -- Requirements for castors for hospital beds
  • ISO 22609:2004 - Clothing for protection against infectious agents -- Medical face masks -- Test method for resistance against penetration by synthetic blood (fixed volume
  • ISO 21171:2006 - Medical gloves -- Determination of removable surface powder
  • ISO 11193-2:2006 - Single-use medical examination gloves -- Part 2: Specification for gloves made from poly(vinyl chloride)
  • ISO 10282:2014 - Single-use sterile rubber surgical gloves -- Specification
  • ISO 8637:2010 - Cardiovascular implants and extracorporeal systems Haemodialysers
  • ISO 8615:1991 - Implants for surgery Fixation devices for use in the ends of the femur in adults
  • ISO 8600 - Endoscopes Medical endoscopes and endotherapy devices
  • ISO 7886 - Sterile hypodermic syringes for single use
  • ISO 7376:2009 - Anaesthetic and respiratory equipment Laryngoscopes for tracheal intubation
  • ISO 7151:1988 - Surgical instruments Non-cutting
  • ISO 1135 - Transfusion equipment for medical use
  • IEC 60601-1 - Medical electrical equipment - Part 1: General requirements for basic safety and essential performance
  • ASTM D7661 - Standard Test Method for Determining Compatibility of Personal Lubricants with Natural Rubber Latex Condoms
  • EN 13612: - Performance evaluation of in-vitro diagnostic devices
  • ISO 4074 - Natural latex rubber condoms Requirements and test methods
  • ISO 7176 - Wheelchairs
  • ISO 8669 - Urine collection bags
  • ISO 5356-1 - Anaesthetic and respiratory equipment -- Conical connectors -- Part 1: Cones and sockets
  • IEEE 1708 - IEEE Standard for Wearable Cuffless Blood Pressure Measuring Devices
  • IEC 60601 - Medical electrical equipment - Part 1: General requirements for basic safety and essential performance
  • ISO 10993 - Biological evaluation of medical devices - Part 1: Evaluation and testing within a risk management process
  • ISO 11137 - Sterilization of health care products - Radiation - Part 2: Establishing the sterilization dose
  • ASTM F1980 - Standard Guide for Accelerated Aging of Sterile Barrier Systems for Medical Devices
  • ASTM 10993 - Biological evaluation of medical devices - Part 5: Tests for in vitro cytotoxicity
  • ASTM - Standard Test Method for Human Repeat Insult Patch Testing of Medical Gloves
  • ASTM F1089-18 - Standard Test Method for Corrosion of Surgical Instruments
  • ASTM F67-13(2017) - Standard Specification for Unalloyed Titanium, for Surgical Implant Applications (UNS R50250, UNS R50400, UNS R50550, UNS R50700)
  • ASTM F75-18 - Standard Specification for Cobalt-28 Chromium-6 Molybdenum Alloy Castings and Casting Alloy for Surgical Implants (UNS R30075)
  • ASTM F451-16 - Standard Specification for Acrylic Bone Cement
  • ASTM F543-17 - Standard Specification and Test Methods for Metallic Medical Bone Screws
  • ASTM F561-19 - Standard Practice for Retrieval and Analysis of Medical Devices, and Associated Tissues and Fluids
  • ASTM F565-04(2018) - Standard Practice for Care and Handling of Orthopedic Implants and Instruments
  • ASTM F623-99(2013) - Standard Performance Specification for Foley Catheter
  • ASTM F640-12 - Standard Test Methods for Determining Radiopacity for Medical Use
  • ASTM F641-09(2014) - - Standard Specification for Implantable Epoxy Electronic Encapsulants
  • ASTM F700-93(2014) - Standard Practice for Care and Handling of Intracranial Aneurysm Clips and Instruments
  • ASTM F702-18 - Standard Specification for Polysulfone Resin for Medical Applications
  • ASTM F719-81(2012) - Standard Practice for Testing Biomaterials in Rabbits for Primary Skin Irritation
  • ASTM F720-17 - Standard Practice for Testing Guinea Pigs for Contact Allergens: Guinea Pig Maximization Test
  • ASTM F732-17 - Standard Test Method for Wear Testing of Polymeric Materials Used in Total Joint Prostheses
  • ASTM F746-04(2014) - Standard Test Method for Pitting or Crevice Corrosion of Metallic Surgical Implant Materials
  • ASTM F748-16 - Standard Practice for Selecting Generic Biological Test Methods for Materials and Devices
  • ASTM F749-13 - Standard Practice for Evaluating Material Extracts by Intracutaneous Injection in the Rabbit
  • ASTM F750-87(2012) - Standard Practice for Evaluating Material Extracts by Systemic Injection in the Mouse
  • ASTM F756-17 - Standard Practice for Assessment of Hemolytic Properties of Materials
  • ASTM F763-04(2016) - Standard Practice for Short-Term Screening of Implant Materials
  • ASTM F813-07(2012) - Standard Practice for Direct Contact Cell Culture Evaluation of Materials for Medical Devices
  • IEC 80601-2-35:2009 - Medical electrical equipment -- Part 2-35: Particular requirements for the basic safety and essential performance of heating devices using blankets, pads or mattresses and intended for heating in medical use
  • ISO 18562-3:2017 - Biocompatibility evaluation of breathing gas pathways in healthcare applications -- Part 3: Tests for emissions of volatile organic compounds (VOCs)
  • ISO 18562-4:2017 - Biocompatibility evaluation of breathing gas pathways in healthcare applications -- Part 4: Tests for leachables in condensate
  • ISO 10282:2014 - Single-use sterile rubber surgical gloves
  • ISO 11193-1:2008 - Single-use medical examination gloves - Part 1: Specification for gloves made from rubber latex or rubber solution
  • ISO 21171:2006 - Medical gloves - Determination of removable surface powder
  • ISO 22609:2004 - Clothing for protection against infectious agents - Medical face masks - Test method for resistance against penetration by synthetic blood (fixed volume, horizontally projected)
  • AS 3695 - Wheelchairs, Part 2: Requirements and test methods for electrically powered wheelchairs (including mobility scooters)
  • AS 4187 - Reprocessing of reusable medical devices in health service organisations
  • AS 4187 - Reprocessing of reusable medical devices in health service organisations
  • ASTM F1980 - Standard Guide for Accelerated Aging of Sterile Barrier Systems for Medical Devices
  • ISO 16755 - ackaging for terminally sterilized medical devices - Guidance on the application of ISO 11607-1 and ISO 11607-2
  • ASTM F2475 - Standard Guide for Biocompatibility Evaluation of Medical Device Packaging Materials
  • ISO 11137 - Sterilization of health care products - Radiation - Part 2: Establishing the sterilization dose
  • ISO 5833 - Implants for surgery - Acrylic resin cements
  • ISO 16402 - Implants for surgery - Acrylic resin cement - Flexural fatigue testing of acrylic resin cements used in orthopaedics
  • ASTM E1061 - Standard Specification for Direct-Reading Liquid Crystal Forehead Thermometers
  • ASTM - Standard Specification for Polysulfone Resin for Medical Applications
  • ASTM E2995 - Standard Specification for ASTM Thermohydrometers with Integral Low-Hazard Thermometers
  • ASTM F1830 - Standard Practice for Collection and Preparation of Blood for Dynamic in vitro Evaluation of Hemolysis in Blood Pumps
  • ASTM F3141 - Standard Guide for Total Knee Replacement Loading Profiles
  • ASTM F3211 - Standard Guide for Fatigue-to-Fracture (FtF) Methodology for Cardiovascular Medical Devices
  • ASTM F2026 - Standard Specification for Polyetheretherketone (PEEK) Polymers for Surgical Implant Applications
  • ASTM F756 - Standard Practice for Assessment of Hemolytic Properties of Materials
  • ISO 14243 - Wear of total knee-joint prostheses
  • ISO 14801 - Dynamic fatigue test for endosseous dental implants
  • ISO 14879 - Total knee-joint prostheses, Part 1: Determination of endurance properties of knee tibial trays
  • ISO 17853 - Wear debris is retrieved and subject to particle analysis
  • ISO 18192 - Wear of total intervertebral spinal disc prostheses
  • ISO 25539 - Cardiovascular implants -- Endovascular devices -- Part 1: Endovascular prostheses
  • ISO 7198 - Cardiovascular implants and extracorporeal systems -- Vascular prostheses -- Tubular vascular grafts and vascular patches
  • ISO 7206 - Implants for surgery -- Partial and total hip joint prostheses -- Part 4: Determination of endurance properties and performance of stemmed femoral components
  • ISO 7206 - Implants for surgery -- Partial and total hip joint prostheses -- Part 6: Endurance properties testing and performance requirements of neck region of stemmed femoral components
  • ISO 7176 - Wheelchairs - Part 10: Determination of obstacle-climbing ability of electrically powered wheelchairs
  • ISO 7176 - Wheelchairs - Part 2: Determination of dynamic stability of electrically powered wheelchairs
  • ISO 14708 - Implants for surgery - Active implantable medical devices - Part 7: Particular requirements for cochlear and auditory brainstem implant systems
  • IEEE 11073 - IEEE Standard - Health Informatics - Personal Health Device Communication - Part 10404: Device Specialization - Pulse Oximeter
  • IEEE 11073-10404-2011 - Health informatics--Personal health device communication Part 10406: Device specialization--Basic electrocardiograph (ECG) (1- to 3-lead ECG)
  • IEEE 11073-10420 - EEE Health informatics -- Personal health device communication Part 10420: Device specialization -- Body composition analyzer
  • IEEE 11073-10421 - IEEE Standard - Health informatics--Personal health device communication Part 10421: Device specialization--Peak expiratory flow monitor (peak flow)
  • IEEE 11073-10422 - Health informatics--Personal health device communication Part 10422: Device Specialization--Urine Analyzer
  • IEEE 11073-19425 - IEEE Health informatics--Personal health device communication - Part 10425: Device Specialization--Continuous Glucose Monitor (CGM)
  • IEEE 11073-10441 - IEEE/ISO International Standard - Health Informatics - Personal Health Device Communication - Part 10441: Device Specialization - Cardiovascular Fitness and Activity Monitor
  • IEEE 11073-10472 - Health informatics--Personal health device communication--Part 10472: Device specialization--Medication monitor
  • IEEE 1708 - IEEE Standard for Wearable Cuffless Blood Pressure Measuring Devices
  • IEEE 2010 - IEEE Recommended Practice for Neurofeedback Systems
  • IEEE 790 - IEEE Guide for Medical Ultrasound Field Parameter Measurements
  • ISO 80601 - Medical electrical equipment-Part2-67:Particular requirements for basic safety and essential performance of oxygen-conserving equipment
  • ASHRAE 11607 - Packaging for terminally sterilized medical devices - Part 1: Requirements for materials, sterile barrier systems and packaging systems
  • ISO 80369 - Small-bore connectors for liquids and gases in healthcare applications - Part 7: Connectors for intravascular or hypodermic applications
  • ISO 11737 - Sterilization of health care products - Microbiological methods - Part 2: Tests of sterility performed in the definition, validation and maintenance of a sterilization process
  • ISO 16146 - Medical devices - Recognized essential principles of safety and performance of medical devices - Part 1: General essential principles and additional specific essential principles for all non-IVD medical devices and guidance on the selection of standards
  • ISO 8536 - Infusion equipment for medical use - Part 4: Infusion sets for single use, gravity feed
  • ISO 60601 - Medical electrical equipment - Part 2-22: Particular requirements for basic safety and essential performance of surgical, cosmetic, therapeutic and diagnostic laser equipment
  • ISO 22442 - Medical devices utilizing animal tissues and their derivatives - Part 1: Application of risk management
  • ISO 11608 - Needle-based injection systems for medical use - Requirements and test methods - Part 1: Needle-based injection systems
  • ISO 11608 - Needle-based injection systems for medical use - Requirements and test methods - Part 1: Needle-based injection systems
  • IEEE C63 - Methods of Measurement for Hearing Aid Compatibility with Wireless Communications
  • IEEE C63 - On-site, Ad-Hoc Test Method for Estimating Radiated Electromagnetic Immunity of Medical Devices to Specific Radio Frequency Transmitters
  • CSA Z316 - Sharps injury protection - Requirements and test methods - Sharps containers
  • CSA C22.2 NO. 80601-2-80:20 - Medical electrical equipment - Part 2-80: Particular requirements for basic safety and essential performance of ventilatory support equipment for ventilatory insufficiency
  • CSA C22.2 NO. 60601-2-31:20 - Medical electrical equipment - Part 2-31: Particular requirements for the basic safety and essential performance of external cardiac pacemakers with internal power source
  • ADA 173 - Designation System for Dental Implants
  • ADA 127 - Dynamic Loading Test for Endosseous Dental Implants
  • ADA 127 - Dynamic Loading Test for Endosseous Dental Implants
  • ADA 46 - Dental Patient Chair
  • ADA 41 - Evaluation of Biocompatibility of Medical Devices Used in Dentistry
  • ADA 130 - Dentifrices - Requirements, Test Methods and Marking
  • ISO 11979 - Ophthalmic implants - Intraocular lenses - Part 5: Biocompatibility
  • ASTM F2884-12 - Standard Guide for Pre-clinical in vivo Evaluation of Spinal Fusion
  • ASTM F1929-15 - Standard Test Method for Detecting Seal Leaks in Porous Medical Packaging by Dye Penetration
  • ASTM F3106-14 - Standard Guide for in vitro Osteoblast Differentiation Assays
  • ASTM F2477-19 - Standard Test Methods for in vitro Pulsatile Durability Testing of Vascular Stents
  • ASTM F1635-16 - Standard Test Method for ?in vitro Degradation Testing of Hydrolytically Degradable Polymer Resins and Fabricated Forms for Surgical Implants
  • ASTM F640 - 20 - Standard Test Methods for Determining Radiopacity for Medical Use
  • ASTM F601-18 - Standard Practice for Fluorescent Penetrant Inspection of Metallic Surgical Implants
  • ASTM F629-20 - Standard Practice for Radiography of Cast Metallic Surgical Implants
  • ANSI Z80.1-2020 - Ophthalmics - Prescription Ophthalmic Lenses - Recommendations
  • ASTM F2212-19 - Standard Guide For Characterization Of Type I Collagen As Starting Material For Surgical Implants And Substrates For Tissue Engineered Medical Products (TEMPs)
  • ASTM F2903-11 - Standard Guide For Tissue Engineered Medical Products (TEMPs) For Reinforcement Of Tendon And Ligament Surgical Repair
  • ASTM F3223-17 - Standard Guide For Characterization And Assessment Of Tissue Engineered Medical Products (TEMPs) For Knee Meniscus Surgical Repair And/Or Reconstruction
  • ASTM F2903-11 - Standard Guide For Tissue Engineered Medical Products (TEMPs) For Reinforcement Of Tendon And Ligament Surgical Repair
  • ASTM E1061-01(2014) - Standard Specification for Direct-Reading Liquid Crystal Forehead Thermometers
  • ASTM F1185-03(2014) - Standard Specification for Composition of Hydroxylapatite for Surgical Implants
  • ISO 10651 - LUNG VENTILATORS - PART 4: PARTICULAR REQUIREMENTS FOR OPERATOR-POWERED RESUSCITATORS
  • ISO 80601 - MEDICAL ELECTRICAL EQUIPMENT - PART 2-74: PARTICULAR REQUIREMENTS FOR BASIC SAFETY AND ESSENTIAL PERFORMANCE OF RESPIRATORY HUMIDIFYING EQUIPMENT

Medical Devices Certifications, Licenses, and Accreditations:

Depending on your Medical Devices products, you may need third-party Medical Devices laboratories or research facilities with specific certifications, licenses or accreditations.

  • FDA
  • MDD
  • USP
  • CMDCAS
  • INMETRO
  • BP
  • JP
  • IEC
  • AIMDD
  • IVDD
  • US FDA
  • GLP
  • GMP
  • QSR
  • EMC
  • CE
  • ASTM
  • AAMI
  • NIST
  • QSR
  • NRTL
  • UKAS
  • BS
  • ISO
  • IEEE
  • A2LA
  • CAEL
  • UL
  • JIS
  • OHSAS
  • ISO/TS
  • WEE
  • RoHS
  • CLIA
  • FDA
  • USP
  • ASTM
  • AAMI
  • AATCC
  • EP
  • GCP
  • UL/ANSI
  • IEC
  • CISPR
  • TUV

Surgical Instrument Cleaning Validation

Caption: Surgical Instrument Cleaning Validation

Medical Equipment Design

Caption: Medical Equipment Design

Wheelchair Testing

Caption: Wheelchair Testing


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