Medical device development varies greatly depending on a variety of factors. It’s important to make sure to always meet the health and safety regulations of the country in which you’ll be distributing your product. Here at Chaban, we have a customizable and comprehensive development strategy for medical devices, making it easy for you to create the exact product you want. We also make sure to meet all regulations necessary for you to meet to manufacture the ideal medical device. That’s why we’re the top choice for Israeli medical device companies.
There are many stages of developing your medical device, from the very conception of the idea to the final product. But today we’re going to focus on how we
develop
the product. Once you know what you want your product to be, have all your ideas in place, and have gotten all necessary investments to start operation (we’ll be with you every step of the way for this process), we then go into our development phase.
Design:
You need a great design to market your product properly. This includes electronic packaging, redesign, and upgrades. We ensure that the design output matches the specified design input and that every decision is verified and validated.
Prototyping:
In this phase, we make an early sample, model, or release of your product, built to test the concept and process so that we’ll all be on the same page when we’re creating the final product.
PCB (printed circuit board) Development:
This process defines electrical connectivity on a manufactured circuit board and is critical to the success of your medical device. We ensure that our PCB development is always up to the highest standards.
Documentation/configuration:
We make sure to document every part of the process in our Medical MRP system, including Product PL, building assembly trees, mechanical drawings, electronic drawings and wirings, and assembly drawings.
Validation:
It’s very important to make sure that your medical device will work the way you intend it to deliver the highest-quality product to your customers. That’s why we conduct damage tests, reliability tests, and life cycle tests. We would never take a chance on your device.
Instruction Writing:
There’s a lot of writing to be done, from the assembly instructions to final test inspections, to the final test report, to packing instructions, and more. We make sure all of that is done so you don’t have to worry about it at all.
Regulation:
Remember what we said about how regulations differ depending on the country? This is where we come in. We support you through the regulation process and provide you with all the information you need to be approved for awards.
DFM (Design for Manufacturing):
We adjust the files for complete compatibility with mass-production technologies like plastic injection, machining while streamlining the assembly, and the maintenance process.
As you can see, there are many phases within the
medical device product lifecycle. From our vast knowledge of engineering to our professional staff, you can be sure that we’ll accompany you from start to finish on your product. Not only that, but once we’ve developed your medical device, we won’t stop there. We have the unique ability to take you to market much faster than the typical manufacturer. This is because we have experience connecting medical devices with resellers and distributors worldwide and making sure that your product gets the market it deserves.
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Main Office
P.O.B 1020, Karmiel 2165373
ISRAEL
Contact
nir@chaban.co.il
+972-4-9981010