PICOCYL的动态

Capital request form changes to prevent medical devices being purchased that you CANT process. Some great tips here. Like ?? and Share. Spread the word and help others out on this.

?? No more redesigns! Drop-in actuators for medical devices. We know the hassle of having to redesign systems to fit new parts. That’s why our drop-in certified actuators for medical devices fit right into your existing setup—saving you time and effort. They’re precise, reliable, and a perfect fit. https://bit.ly/3zEi1ir

To all legacy and "ex class I" devices manufacturers: Time is running out. This is the last call for all those manufacturers who need a NB urgently. How many Notified Bodies are still able to accept your application less than 1 month to the expiry date??? We can do that and we can accept your application and manage the transitional period despite the few time!!! With us you can still hope to place your device on the market till Dec 2027 or 2028 based on the risk class. Don't be complicit in your own business failure, but especially in the absence of your medical devices on the market, to the detriment of patients. Don't hesitate anymore and write me at: [email protected]

On January 1, 2025, an amended Executive Order on Medical Devices entered into force, which makes it possible to send single-use medical devices for reprocessing and further reuse. At the same time, it ensures that the reprocessed devices are safe and effective to use on an equal footing with the original CE-marked devices: https://lnkd.in/eBY2xG8Y

When choosing a quick disconnect connector for a medical device, there are eight important factors that should be considered. Learn how compatibility, sterilization, durability and safety play a critical role in ensuring device functionality. ? Read More: https://bit.ly/3wyzLcN ? #qosina #medicaldevices #medtech #medicaldevicemanufacturing

PUI introduces its new buzzers specifically designed for medical devices! With ever-increasing quantities of medical equipment inside and outside clinical environments, PUI Audio understands our customers’ needs for a reliable, easy-to-use component. PUI set out to give engineers the ability to quickly and effectively certify their devices for IEC 60601-1-8 compliance - and now are introducing the latest expansion of our Audio Indicators - Medical Indicators. Availability: Parts will be in stock by mid-December, and sample quantities are available! Resources: Specification: https://buff.ly/4i6I17b Release Document: https://buff.ly/3CD6zV9 Application Guide: https://buff.ly/499oG12

On January 1, 2025, an amended Executive Order on Medical Devices entered into force, which makes it possible to send single-use medical devices for reprocessing and further reuse. At the same time, it ensures that the reprocessed devices are safe and effective to use on an equal footing with the original CE-marked devices: https://lnkd.in/eEVsnKbP

Learn about cleaning validation with this episode. Don‘t miss the discussion I had with Heena Thakkar

Download our Medical Device Compatibility Guide and explore how #supercriticalCO2 sterilization can safely and effectively sterilize Combination, Implantable, Topical, and Electronic devices: https://bit.ly/3S6SKnf

?? HOT NEWS??High-level EU moves are afoot to try and scrap the 5-year notified body review for Class IIa and the majority of Class IIb devices, and extend the review time from 5 to 10 years for Class III devices and Class IIb implantables. This and other far-reaching changes are being considered at European insitution level. #EUMDR #medtech https://bit.ly/4bOWIrE