Autologous Blood Salvage Device
5,000 Per Piece
100 Piece (MOQ)
Product Features Modularised design enables fast and safe handling of emergencies Offers affordable yet state of art solutions for harvesting blood components with down stream therapy specific filters Easy to setup and Easy to dismantle User-friendly and detachable filtration & storage modules Click-O-lock connector for blood bag attachment & detachment Contamination free handling of blood from surgical site to filtration, collection & storage Vacuum assisted transfer enables fast filtration & collection Facilitates on-line mixing of anticoagulant, if required Biocompatible Materials meets USP Class VI standards Crystal clear parts enable best viewing
Containment Transfer Devices
200,000 - 300,000 Per piece
10 p (MOQ)
Rapid transfer Port system is recognized as being the safest method for bidirectional transfer in aseptic or toxic working areas, without breaking containment or sterility. The port can be fixed onto the cleanroom, filling line, or isolator wall. Alpha units installed worldwide, its reliability and safety have set it as the industry standard. Leak tight transfer Reliable and safe transfer Total solution with Beta parts and accessories Validated solution A large variety of applications The Alpha part is mounted on a support – commonly an isolator, RABS, BSC, or cleanroom. The Beta part consists of a container, bag, or other Beta device used for the transfer of components, solids, or liquids. The Alpha parts and Beta parts are connected by a manual 60° rotation which detached the doors from their supports and joins them together. Tightness is secured by the lip seals of the new assembly. The doors can now be opened without breaking sterility or containment. The combination of Alpha and Beta parts is a validated solution. Used together, they provide highly secure transfer and protect your production.
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ISO 13485 Medical Devices Quality Management
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From Delhi (India), we are a credible ISO 13485 Medical Devices Quality Management Service provider. The ISO 13485 Medical Devices Quality Management that we render is adequate and reliable. Our team of adroit professionals manages all the work to ensure the service is executed with 100% perfection and that too within the promised time period. The paper work is carried out with full attention and responsibility, so that the clients do not face any problem. Details : QSC has the capability and resources to support companies throughout the process of developing an effective Quality management for medical devices certification Program, performing independent audits of compliance-related processes and controls, and reporting on results. ISO 13485 is based on the ISO 9001:2008 process model approach and is a management systems standard specifically developed for the manufacture of medical devices. Its primary objective is to facilitate harmonized medical device regulatory requirements. The standard contains specific requirements for manufacture, installation and servicing and calls for: Implementation of a Quality Management System with several enhancements Risk Management approach to product development and product realization Validation of processes Compliance with statutory and regulatory requirements Effective product traceability and recall systems.
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We are engaged in providing our clients mobile device management system. a mobile devices management is emerging solution from smb to corporate. We have proven expertise in delivering mdm solution effectively. These systems are are made accordance with a international quality standard and norms. features: solution is compatible with android handsets highly scalable cloud application with advance user interface & user experience various software versions as per consumer and corporate requirement almost all mobile functionality controllable and manageable from cloud provides phone security along with its location tracking.
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Medical Device Quality Management System Iso 13485