Manufacturers Service

Innokas Medical Ltd.

Vihikari 10 , 90440 Kempele
Finland

Telephone +358 8 5623100
innokas@innokasmedical.fi

This company is co-exhibitor of
Wulff Entre Oy

Trade fair hall

  • Hall 15 / B05
 Interactive Plan

Hall map

MEDICA 2016 hall map (Hall 15): stand B05

Fairground map

MEDICA 2016 fairground map: Hall 15

Our range of products

Product categories

  • 01  Electromedical equipment / Medical Technology
  • 01.04  Intense medicine / anesthesiology / respiration
  • 01.04.04  Patient monitoring systems / Measuring stations

Patient monitoring systems / Measuring stations

Our products

Product category: Patient monitoring systems / Measuring stations

LCM Manufacturing

Product life cycles are managed in the manner specified in Innokas Medical’s quality system so that they meet the official regulations and standards set for medical and in vitro devices.

Everything stems from a satisfied end customer, which may be a doctor, a hospital staff member, or a hospital maintenance person. As the age of a product increases, it becomes necessary to carry out maintenance procedures. In some cases these procedures involve processing a customer complaint, which may lead to a product revision or even an on-site technical update of the product. Innokas Medical can do all of this for our customers in a manner specified in our quality system and approved by officials.

As the age of a product increases, the need for maintenance procedures grows, and in some cases it is necessary to carry out updates due to changes in the environment. If ROHS or other similar needs so dictate, our maintenance planning and documentation offer product revisions and product documentation updates. Product data are managed within Innokas Medical’s systems, or if a customer so desires, they are updated directly within the customer’s product data management system.

Life cycle management philosophy is a very important part of producing health technology and manufacturing healthcare devices. We at Innokas Medical understand this — we have done it already since 1994.

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Product category: Patient monitoring systems / Measuring stations

R&D Services

Contract Design for Medical Devices

We are specialized in medical technology design services. Innokas designs high-quality medical devices from idea conceptualization through device development until transfer to production. Our design process covers the entire medical device development taking care of efficient project control, risk management and Device Master Record (DMR) documentation following FDA (510k), MDD (CE) and other regional regulatory requirements. Our core competencies cover all necessary disciplines such as electrical engineering, mechanical engineering, embedded and client software development, user interface and usability design, industrial design, tester design, prototyping, verification and validation as well as quality and risk management.

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Product category: Patient monitoring systems / Measuring stations

LCM Engineering

Product life cycles are managed in the manner specified in Innokas Medical’s quality system so that they meet the official regulations and standards set for medical and in vitro devices.

Many of our customers have outsourced product maintenance to Innokas, freeing resources for new product development. Strict regulatory requirements must also be met in the maintenance phase of medical devices, and therefore Innokas is a natural partner. We routinely take full responsibility for all service and maintenance even if the design of the particular device was not created by Innokas.

Our services in the product maintenance phase include:
Installation-based support, including regular maintenance
Device Master Record maintenance, including redesign and revision control management
Handling of complaints
Technical/customer support
Product end-of-life management
Cost reduction (e.g., redesign or consolidation of suppliers)

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About us

Company details

Innokas Medical - Your co-creation partner in medical technology!

We have lived for healthcare technology for over 20 years. Since 1994 we’ve improved the quality of peoples’ lives by crafting healthtech ideas to reality.

We transform our customers’ ideas into a high quality products. With us you can experience the agile path from idea to regulatory approvals and cost-efficient manufacturing of your medical device.

Our HQ is in Oulu area, Finland, and our other sites are in Helsinki, Finland and in Tallinn, Estonia. Company quality management system has ISO13485 & Canada ISO13485 Certifications and FDA registrations which makes us the preferred co-creation partner for medical OEMs all over the world!

You have an idea of a Medical Device? Let’s realize it together!

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Company data

Sales volume

10-49 Mio US $

Number of employees

100-499

Foundation

1994

Area of business
  • Electromedical equipment / Medical Technology
  • Diagnostics
  • Medical Services and Publications