sdk_imported
Mechanical
- May 16, 2002
- 49
I am new to injection molded medical devices. I am designing a plastic part that will go inside a person's mouth.
The part must satisfy the ISO 10993 biocompatibility standards (cytotoxity, sensitization, and irritation). I would like to start by doing some prototype molding for clinical testing.
Here are my question:
(1) If I mold prototpyes in a clean (not "clean room") environment and then follow a simple cleaning protocol, will the device satisfy this biocompatibility requirements per ISO 10993?
(2) Is it really necessary to have a lab run biocompatibility testing on the parts before using them on people? The test takes roughly 2 months at a cost of about $10k.
I would appreciate any feedback from an injection molder of finished products that are FDA class 1 medical devices.
Thanks in adavance.
The part must satisfy the ISO 10993 biocompatibility standards (cytotoxity, sensitization, and irritation). I would like to start by doing some prototype molding for clinical testing.
Here are my question:
(1) If I mold prototpyes in a clean (not "clean room") environment and then follow a simple cleaning protocol, will the device satisfy this biocompatibility requirements per ISO 10993?
(2) Is it really necessary to have a lab run biocompatibility testing on the parts before using them on people? The test takes roughly 2 months at a cost of about $10k.
I would appreciate any feedback from an injection molder of finished products that are FDA class 1 medical devices.
Thanks in adavance.