This website contains safety and performance information of products manufactured by Terumo Europe N.V. that are certified under the Medical Device Regulation (EU) 2017/745 (Annex I, chapter III, 23.1 general requirements)
To consult the Patient Information Leaflets for Australia, please click here.
Revision 2
In this document you will find safety and performance information as covered in the Instructions for Use for the product: RADIFOCUS™ Guide Wire M Non-Vascular - Non-vascular guide wire
In this document you will find safety and performance information as covered in the Instructions for Use for the product: K-Pack Surshield™ Needle
In this document you will find safety and performance information as covered in the Instructions for Use for the product: Ultimaster Nagomi™ Sirolimus eluting coronary stent system
In this document you will find safety and performance information as covered in the Instructions for Use for the product: Surflo™ Winged Infusion Set with Needle Protection
In this document you will find safety and performance information as covered in the Instructions for Use for the product: Surflo™ Winged Infusion Set with Filter and Needle Protection
Revision 1
In this document you will find safety and performance information as covered in the Instructions for Use for the product: RADIFOCUS™ Introducer II - Introducer for radial access
In this document you will find safety and performance information for the product: K-Pack™ II Needle
In this document you will find safety and performance information for the product: Neolus™ Needle
In this document you will find safety and performance information as covered in the Instructions for Use for the product: SurGuard™3 Safety Hypodermic Needle
In this document you will find safety and performance information as covered in the Instructions for Use for the product: Terumo Injection Filter Needle
In this document you will find safety and performance information as covered in the Instructions for Use for the product: K-Pack Embrace™ Active Safety Needle
In this document you will find the Magnetic Resonance Imaging (MRI) conditions to allow safe scanning of your patient implanted with Ultimaster Nagomi™ Sirolimus eluting coronary stent system.
In this document you will find all relevant information on your implant: Ultimaster Nagomi™ Sirolimus eluting coronary stent system
In this document you will find safety and performance information as covered in the Instructions for Use for the product: Terumo Syringe with Fixed Needle Gonal-f Multi-Dose 600 IU/ml FSH
In this document you will find safety and performance information as covered in the Instructions for Use for the product: Terumo Syringe with Fixed Needle MENOPUR Multidose 600 IU/ml FSH/LH
In this document you will find safety and performance information as covered in the Instructions for Use for the product: Terumo Syringe with Fixed Needle 600 IU/ml FSH
In this document you will find safety and performance information as covered in the Instructions for Use for the product: Terumo Syringe with Fixed Needle Folisurge 600 IU/0.96ml FSH
In this document you will find safety and performance information as covered in the Instructions for Use for the product: Terumo Syringe with Fixed Needle 1 mg/0.2 ml leuprolide acetate
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Document content may be subject to change.
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