- Home
- Services
- north korea
- medical device test
Refine by
Medical Device Test Services Available In North Korea
18 services found
by:Protheragen-ING based inNEW YORK (USA)
Reusable medical devices, such as surgical instruments, endoscopes, and anesthesia equipment, offer a cost-effective and environmentally friendly alternative to disposable devices. However, the complexity of these devices, coupled with the potential for biofilm formation and residual contamination, presents unique challenges in ...
by:STEMart based inShirley, CALIFORNIA (USA)
An active implantable medical device (AIMD) is any active medical device that is intended to be totally or partially introduced, surgically or medically, into the human body or by medical intervention into a natural orifice for diagnostic or therapeutic purposes, and which is intended to remain in place after the procedure. Since AIMDs are engineered to maintain direct contact with the body for ...
by:Test Labs Ltd based inPeterborough, UNITED KINGDOM
Test Labs Ltd provides comprehensive accelerated and real-time aging testing services to evaluate the stability of products under various storage and use conditions. Accelerated aging testing simulates long-term aging processes by exposing products to elevated stress conditions, such as increased temperature and humidity, over a shorter period. ...
by:Test Labs Ltd based inPeterborough, UNITED KINGDOM
Test Labs Ltd provides a Medical Device Cleaning Validation service that ensures medical device cleaning protocols, as specified in the Instructions for Use (IFU), are accurately validated. This service is applicable to both manual and automated cleaning methods and complies with international standards such as ...
by:Emmace Consulting AB based inLund, SWEDEN
Testing and determination of Particulate Matter (PM) and Volatile Organic Substances (VOS) according to ISO 18562-2 and ISO ...
by:Emmace Consulting AB based inLund, SWEDEN
ISO 18562-4 addresses the critical need for quantifying and assessing the risks associated with condensate produced during patient use, which can potentially enter the lungs or the throat region depending on the device. Accurate measurement of the condensate volume is essential for ensuring patient safety, meeting regulatory requirements and making it possible to estimate the exposure to ...
by:STEMart based inShirley, CALIFORNIA (USA)
Cytotoxicity testing is a sensitive method to assess the biocompatibility of a material extracted through a specific cell culture media following exposure of the extracted fluid to L929 cells. This test is performed on raw materials in the manufacturing process, all medical devices contacting patients, and ...
by:STEMart based inShirley, CALIFORNIA (USA)
STEMart performs a variety of testing for partial and total hip joint prostheses to measure how they will withstand different levels of fatigue, compression, torsion, and bending over an extended period of time. ...
Manufactured by:Sanbor Medical based inAllentown, PENNSYLVANIA (USA)
Sanbor Medical offers a full range of medical device testing and programming capabilities to help our customers delight their users and succeed long-term. ...
by:IMR Test Labs based in
Our Mechanical Fatigue Testing Services Laboratories utilize cyclic loading (HCF-LCF) to predict the life of materials under fluctuating loads and temperatures. Determining fatigue life can support research and development efforts for new materials as well as prevent failures and recalls when used to ensure material properties. Understanding a material fatigue life is critical in ...
Manufactured by:SRT-Microcéramique based inVENDOME, FRANCE
Burn-in testing is a service designed to identify any potential defects in electronic components before they are dispatched to customers. This testing process subjects the components to thermal cycling and power cycling to simulate extreme operational conditions. The primary goal is to catch weak components that could fail prematurely during normal use, which ...
by:STEMart based inShirley, CALIFORNIA (USA)
Processes close or equal to those to be used in production. Pilot production is a crucial process for devices that will be tested in clinical trials or pilot markets before transitioning to full-scale production. If the customer’s medical device is successful in a pilot market or clinical trial, it will likely transition to ...
Manufactured by:DemeTECH Corporation based inMiami Lakes, FLORIDA (USA)
DemeTech’ s R&D Department will design, develop, prototype medical device ideas. After testing and proof of concept, we can develop final production models and provide scalability for mass ...
by:Protheragen-ING based inNEW YORK (USA)
The safety and effectiveness of medical devices are of paramount importance in the healthcare industry. Before these devices are approved for use, they must undergo rigorous testing to ensure that they meet the necessary safety standards. Protheragen-ING Lab specializes in providing comprehensive and reliable ...
Manufactured by:MediPurpose based inDuluth, GEORGIA (US) (USA)
The MediPurpose™ Medical Device Innovation division collaborates with medical device inventors and innovators to take new medical devices from concept to commercialization—bringing together financing, proven medical device development methodology and global experience to help ensure success. Taking a new medical invention from concept to commercialization can be a difficult process, ...
Manufactured by:Ceutical Labs based inFlower Mound, TEXAS (USA)
There are several distinct markets that are served by the Analytical Testing Division. They include Pharmaceutical, Nutraceutical, Medical Device, API (Active Pharmaceutical Ingredient), NDI (New Dietary Ingredient) and Post Sterilization Testing. Two of these categories, API and NDI require additional explanation. ...
Manufactured by:Bastos Viegas, SA based inGuilhufe, PORTUGAL
Bastos Viegas SA always had and still has as one of its main objectives produce high quality and meeting the requirements of its customers and the market in general as well as all applicable legal requirements. Therefore Bastos Viegas bet on the implementation and constant updating of a quality control system that currently has decades of experience. In this sense always equipped its laboratories ...
by:Life Science Outsourcing, Inc. based inBrea, CALIFORNIA (USA)
The medical device packaging design, testing, and validation process can be intricate and time-consuming, facing intense regulatory scrutiny and often being the largest cause of FDA recalls. Starting medical device packaging validation too late in the design process can create significant challenges for most ...