Technology at the edge of the possible
1995
Research begins in quantum technology, biophysics, and the subconscious.
2001
The company is registered as Alfa-Med LLC, headquartered in Moscow.
3
Production and testing sites: Skolkovo Innovation Center, Setun, and Omsk.
2
International partners: TESLA joint-stock company Hloubetin and LG SeoulTech joint-stock company Seoul.
Diagnostic systems detect health problems, find the underlying cause, and recommend the best path to recovery.
Certificates
Official company documents and licenses
We use a five-step quality control process (5SI)
- The SENSITIV IMAGO trademark is registered in the USA and other countries
- The SensitivE Audit trademark is registered in the USA and other countries
- Russia Certificate 2020 for Sensitive Audit 551, DL
- Medical Device Establishment Licence. Health Canada
- Egyptian Ministry of Health Central Administration for Pharmaceuticals General Administration for Pharmaceutical Licensing Importers Department License Registration
- Certificate of the Central Department of Pharmacy of the Ministry of Health of Egypt.
- Certificate_EC part A Annex III directive 2014/30/EU 2018_SensitivE Audit model 550. Monitoring non-vital physiological parameters
- Certificate Registration FDA 2018 Sensitive audit 555 is registered and has listed the following medical device with the US
- Certificate Registration FDA 2016-2021 Sensitiv imago 535, 135
- EU 2016 certificate CE 530, 130.
- Certificate of the Russian Federation Customs Union 2015-2020 Express Test System Sensitiv imago 7 models.
- RF Certificate 2009 for 9 Sensitiv Imago Models
- European Certificate corresponding Class 2- medical equipment. The certificate was obtained for 4 models
- Identification certificate of the UK for 3 models manufactured by medical Class 1. Testing laboratories, test performed in UK according to the EU standards
- Device Certification in Ukraine
- Certificate for Latvia
- Declaration
- International Certificate of production according to ISO 9001: 2008 Rus standards and the latest directive of 2014
- European International Certificate for manufacturig, development, design, scientific activity according to the ISO 9001:2008, revision 2014
- Certificate of quality management 13485 issued by the European Union for the production and design of medical devices
- Certificate of the management system for the production of medical equipment in accordance to EU Standard 13485
- Registering Lifestream software in the United States
- Hygienic Certificate of the manufacturer Russia
- Certificate for the line of equipment of the Ministry of Emergency Situations of the Russian Federation
- Certificate confirming the performing of the audit for the right to manufacture medical equipment in accordance to the 2014 directives
- Certificate confirming the audit for the right to develop medical equipment under the 2014 directives
- Testing devices in the German laboratory TUV
- Laboratory Tests in EU 2016 LEI
- EMC tests on medical parameters 60601_1_2
- IEC 60601-1:2005 Medical electrical equipment
- Registration of a factory for the USA
- Trademark Registration SENSITIV I M A G O priority from 2005
- Registration of the brand SENSITIV IMAGO priority from 2011
- Trademark Registration LifeStream priority from 2012
- Brand registration IMAGO TECHNOLOGY priority from 2012
- Registration of the brand SensitivE imaGO priority from 2017
- Registration of the brand SensitivEGO priority from 2016
- Registration of the brand SensitivE Audit priority from 2018
- Registration of the brand ALFA-MED priority from 2019
- Diploma to the Gold Medal of the European Union in the field of development of innovative technologies
Information about the 5SI Quality Standard
– Every ALFA-MED device undergoes a complete cycle of testing — from design through delivery to the customer. This is how we ensure the safety and accuracy of research conducted on Sensitiv equipment.
– Quality is built in at the design stage. The earlier we identify weaknesses, the fewer modifications are needed in subsequent versions. The result: the device's specifications match customer expectations.
– ISO Certification. Our manufacturing processes are certified according to international ISO standards, recognized worldwide.
– Statistical Process Control (SPC). We continuously monitor production parameters, identify sources of deviation, and prevent them from becoming embedded in serial production.
– Technology. ALFA-MED devices outperform existing bioresonance diagnostic and wellness methodologies in their specifications. Competitors' equipment reproduces only a fraction of the functions built into our technology.
– Customer Focus
Our goal is to ensure customers are satisfied with their device and receive a competitive product for their investment. We measure the value of our equipment by two metrics: how much it is needed by consumers and how well it is made.
– Personnel
We invest in training our employees across all company divisions — from manufacturing to after-sales service.
– After-Sales Service
For many clients, the availability of service support becomes the deciding factor when choosing a device. Our specialists support the equipment throughout its operational life and continuously gather feedback from users.
– Suppliers
Over years of manufacturing medical equipment, we have developed our own system for evaluating components. This has allowed us to reduce the number of suppliers and improve the quality of finished products.
– Quality is built in at the design stage. The earlier we identify weaknesses, the fewer modifications are needed in subsequent versions. The result: the device's specifications match customer expectations.
– ISO Certification. Our manufacturing processes are certified according to international ISO standards, recognized worldwide.
– Statistical Process Control (SPC). We continuously monitor production parameters, identify sources of deviation, and prevent them from becoming embedded in serial production.
– Technology. ALFA-MED devices outperform existing bioresonance diagnostic and wellness methodologies in their specifications. Competitors' equipment reproduces only a fraction of the functions built into our technology.
– Customer Focus
Our goal is to ensure customers are satisfied with their device and receive a competitive product for their investment. We measure the value of our equipment by two metrics: how much it is needed by consumers and how well it is made.
– Personnel
We invest in training our employees across all company divisions — from manufacturing to after-sales service.
– After-Sales Service
For many clients, the availability of service support becomes the deciding factor when choosing a device. Our specialists support the equipment throughout its operational life and continuously gather feedback from users.
– Suppliers
Over years of manufacturing medical equipment, we have developed our own system for evaluating components. This has allowed us to reduce the number of suppliers and improve the quality of finished products.
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