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Promepla OEM Solutions has 20 years experience in Manufacturing, Assembly and Packaging of Single Use Medical Devices. Promepla has experience in assembly of complex devices for the pharmaceutical, drug delivery, medical and healthcare industries.
Cleanroom Facilities include
Two (ISO class 8 / US class 100 000) cleanrooms over 2 000 sq meters for assembly and packaging.
One (ISO class 8 / US class 100 000) cleanrooms over 200 sq meters for injection.
Cleanrooms certified to ISO 14644 for airborne particulate
Possibility to work under a more restrictive environnement if requested or necessary. (ISO7 or less)
Micro organism monitoring (on product, surfaces and air) ensures environment compliance and future sterility of the product.
Our manufacturing capabilities include:
Precision injection moulding
Flexible assembly solutions – pilot production to high volume
Multi solvent bonding
Drilling, cutting & welding
Adhesive & UV bonding
Multi-colour pad printing
Hard and soft packaging
Leider gibt es für diesen Aussteller kein deutsches Firmenprofil.
Promepla OEM solution is an established and experienced company specialised for almost 50 years in single-use medical devices design, development and manufacture. Our team of 250 people is completely dedicated to serving the medical industry with the highest standarts:
→ CONTRACT MANUFACTURING
Promepla provides you the turnkey solution to the specific needs of your market.
Our expertise goes through the most diverse medical sectors such as Angiography, Ophtalmology, Dental, Cardiology, Biopharm and many other.
→ FLUIDMANAGEMENT COMPONENTS
Promepla povides you a large selection of OEM USP class VI components to the medical and pharmaceutical industry.
Our product line includes Neuraxials, Luer, Check valves, Connectors, Stopcocks, Torquers, Clamps, Spike, Injection site, Tuohy borst, Tubing etc.
→ RESEARCH AND DEVELOPMENT
Our team of qualified engineers, expert in materials, manufacturing and our technicians will bring your projects to life by offering a high quality of service.
Our Quality and Regulatory team will accompany you to bring your medical devices to the world market, taking care of the different stages of verification, validation and interaction with the competent authorities.