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The guidance behind every application.
Instructions for Use (IFU) for JULÄINE™, providing essential information for the safe and intended use of the medical device.
Guidance you can rely on.
Select the country and language below to access the applicable Instructions for Use for JULÄINE™. Ensure that the Instructions for Use correspond to the product reference you are using.
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Instructions for Use (German)
Reconstitution, application and safety information for use in your practice.
DownloadCommitted to quality and safety.
JULÄINE™ is certified in accordance with Regulation (EU) 2017/745 on medical devices (MDR), demonstrating conformity with applicable requirements relating to safety, performance, clinical evaluation and post-market surveillance.
At Nordberg Medical, our commitment to quality extends throughout the product lifecycle — from development and manufacturing to the information we provide to healthcare professionals. Our quality management system is certified to ISO 13485:2016, the international standard for quality management systems in the medical device industry.
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