MedTech and Instrumentation
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PartnerTech has as a contract manufacturer a long history of success in the medical device and medical technology industry. We can help you develop and manufacture equipment and instruments that meet the rigorous regulatory standards in Europe, Asia and the United States. With a global network of manufacturing facilities across Europe, China and the Unites States and state-of-the-art facilities, PartnerTech can support you through your product’s entire life cycle.
We use the ISO 13485 Medical Device Quality Management Standard as the benchmark for our regulatory requirements. We adapt our processes to meet the requirements for medical device manufacturing, the Quality System Regulation (QSR) in the United States, the Pharmaceutical Affairs Law (PAL) in Japan, and the Medical Device Directory (MDD) and In Vitro Diagnostic Device Directive (IVDD) for Europe.
- Product design and development
- New product roll-outs
- Development of mechanics and fluids
- Warehousing, logistics and spare parts maintenance
Accreditations and standards
- ISO 9001
- ISO 14001
- ISO 13485
- QSR (USA)
- PAL (Japan)
- MDD (Europe)
- IVDD (Europe)
Blood analysis equipment, radiology and anesthesiology equipment models, mechanical heart compressions systems, dialysis equipment, allergy testing equipment, DNA analysis equipment and prostate treatment equipment.