PDT LASERS
For activation of Photosensitizers intended for the Treatment of Cancer.
Omicron offers laser systems for PDT applications in combination with common or new photosensitizers.
The systems are equipped with all required functionalities for usability and safety.
ISO CERTIFIED PRODUCTION
Omicron designs and manufactures medical lasers
according to ISO 13485:2016 with technical approval
according to the EN (IEC) 60601-1 (Edition 3.1)
standard. Further the design complies to FDA/CDRH 21
CFR 1040.10 and Japanese PMDA standards.
WHY OMICRON?
Omicron-Medical is a department of Omicron-Laserage Laserprodukte GmbH, a laser manufacturer with 35 years of experience in the field of developing and producing industrial lasers and systems for LifeSciences and more. Fore further information, click here.
Customized Solutions
Omicron supports any kind of customized solutions. Developing new products or adapting existing designs to customer´s requirements is one of the core capabilities. From prototype to serial production, Omicron is your competent partner.
High- Competence Consulation
With more than 30 years of experience in industrial laser technology and over 10 years as a manufacturer for medical laser systems Omicron provides comprehensive advice for various challenges in the market.
Reliable Partner
Being a reliable partner in long term business relations or supporting start-ups, Omicron helps and consults during standard processes and challenging new upcoming projects.
❝ The benchmark for the quality of our products and services is determined by the
customer. Their judgement is decisive. Through our knowledge and know-how of
medical devices, we have a moral obligation to develop and manufacture them for
the benefit of patients. ❞
COMPANY PHILOSOPHY
Our wishes
- Deliver customized solutions for individual requirements
- Provide customized support
- Always be one step ahead of competitors
- Bring a new development to the market twice a year
- Be a technology leader develop „unique“ products
- Offer exceptional after sales support
- Provide individual demonstration systems
For the purpose of
- Being perceived by our customers as a friendly, customer-oriented company, which works in accordance with their interests and delivers high-quality products
- Being regarded as a reliable partner for customers and suppliers at home and abroad
- Building long-lasting and stable relationships through high customer satisfaction
We achieve this by
- The quality of our products and services
- The ability to work in a team
- A friendly approach to our customers,suppliers and colleagues
- Efforts to constantly improve ourselves and our processes within the company
OMICRON MEDICAL JAPAN
Omicron Medical Japan is a branch establishment representing Omicron Medical products exclusively in Japan. The operating base is located in Tokyo. OMJ is
officially licensed by the Japanese authorities to service and repair all medical products.
OMICRON TECHCAMP
Omicron introduces the new inhouse TechCamp. As an institution for seminars, workshops and product presentations the TechCamp comes up with high tech equipment like advanced meeting rooms as well as
movable and flexible glass walls for larger conferences. Customers and partners can explore product service, a complete microscopy room and an entire virtual reality operating theatre.
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PDT Laser Systems
1-channel
2-channel
4-channel
- Intuitive control via touch screen user interface
- Output-channels upgradable to maximal system configuration
- Fibre port for flexible adaption to common connector types and light-distributors
- Precise and homogenous treatment beam
- Auto calibration port for sterile inserts (CPI)
- Treatment parameters set by auto-calculation or manual adjustment
- Individual adjustment of irradiance
- Recording data for treatment documentation (USB-PC connection)
- Low noise operation
ISO CERTIFIED PRODUCTION
Omicron designs and manufactures medical lasers
according to ISO 13485:2016 with technical approval
according to the EN (IEC) 60601-1 (Edition 3.1)
standard. Further the design complies to FDA/CDRH 21
CFR 1040.10 and Japanese PMDA standards.