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You will find here electronic copies of safety and performance information for selected Terumo products to which EU-Medical Devices Regulations and In Vitro Diagnostic Regulationhas been applied. All documents are available for download as PDF files. To read them, you must have Adobe Reader installed on your computer.
If necessary, click here to download Adobe Reader for free. The version of the Instruction Manual that you should refer to depends on what product you received.
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e-IFU
You will find here electronic copies of Instructions for Use for selected Terumo products to which European Regulation No. 207/2012 has been applied.
You can download the actual Instruction Manual for your product, up to 15 years at least after purchase.
All documents are available to download as PDF files. To read them, you must have Adobe Reader* installed on your computer.
If necessary, click here to download Adobe Reader for free.
Please contact Terumo to receive a printed copy of one of the listed e-IFU's within 7 days.
The version of the Instruction Manual that you should refer to depends on what product you received.
Please check the Serial Number or lot number of your product to determine the version that goes along with it.
IC
Implant card
e-IFU
You will find here electronic copies of Instructions for Use for selected Terumo products to which
European Regulation No. 207/2012 has been applied.
You can download the actual Instruction Manual for your product, up to 15 years at least after purchase.
All documents are available to download as PDF files. To read them, you must have Adobe Reader*
installed on your computer. If necessary, click here to download Adobe Reader for free.
Please contact Terumo to receive a printed copy of one of the listed e-IFU's within 7 days.
The version of the Instruction Manual that you should refer to depends on what product you received.
Please check the Serial Number or lot number of your product to determine the version that goes along
with it.

Disclaimer

Safety and performance information of TERUMO products based on EU-Medical Devices Regulation and In Vitro Diagnostic Regulation is available in this website.
Not all of the Terumo products shown on this website are registered in, approved for sale in, or available for purchase in, all countries or regions where this website is accessible. Specific indications for use may vary by country and region.
The contents of the IFU may be subject to change without prior notice. Please consult with your local Terumo representative, distribution company or customer service center for additional information.

Are you a European healthcare professional, or a patient using implant products?
The content of this website is reserved for those only.

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