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Eckert & Ziegler Strahlen- und Medizintechnik AG

Regulatory Filings Apr 23, 2015

130_rns_2015-04-23_bcdd10f8-c65f-47d6-8486-d41cb76a66c3.html

Regulatory Filings

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News Details

Corporate | 23 April 2015 07:45

Eckert & Ziegler’s SagiNova(R) afterloader receives FDA market clearance

Eckert & Ziegler Strahlen- und Medizintechnik AG / Key word(s): Regulatory Approval

2015-04-23 / 07:45


Press release

Eckert & Ziegler’s SagiNova (R) afterloader receives FDA market clearance

Berlin, April 23, 2015. Eckert & Ziegler has received market clearance from the U.S. Food and Drug Administration (FDA) for its new SagiNova (R) afterloader. The receipt of approval marks yet another milestone in the company’s expansion in the U.S. brachytherapy market. North America is the largest homogeneous market for brachytherapy, a form of radiation therapy that applies radiation directly on the tumor location. Almost 40 % of all tumor irradiation equipment installed worldwide is located at the 2,400 radiation therapy centers in the U.S. Temporary brachytherapy is especially widely used for gynecological applications. However, its wide range of potential applications also allows it to be used on other forms of cancer.

“Eckert & Ziegler BEBIG and Mick Radio-Nuclear Instruments, a U.S. company that we acquired in 2013, have decades of experience in the field of HDR technology. We estimate the annual market volume for tumor irradiation systems in the U.S. to be almost EUR 50 million, and we’re happy to play an increasingly important role in this market,” says Dr. Edgar Löffler, Member of the Executive Board of Eckert & Ziegler AG in charge of the Radiation Therapy segment.

SagiNova (R) is the only brachytherapy afterloader available with both a Co-60 and an Ir-192 source with 510(k) approval.

HDR brachytherapy involves placing a miniaturized radiation source in the tumor site for a short period of time and is an integral part of cancer treatment. Patients often receive HDR brachytherapy as a stand-alone treatment or in combination with external radiation therapy or chemotherapy. Based on the age-standardized number of new cases per 100,000 inhabitants, 25 % more people develop cancer in the U.S. than in Europe.

SagiNova (R) will be unveiled to the public at ESTRO Forum, the annual conference of the European Society for Radiotherapy & Oncology, in Barcelona (April 24-28, 2015).

SagiNova (R) was awarded a CE mark in late 2014.

About Eckert & Ziegler

With around 700 employees, Eckert & Ziegler Strahlen- und Medizintechnik AG (ISIN DE0005659700) is one of the world’s largest providers of isotope technology components for radiation therapy and nuclear medicine.

Contributing to saving lives

For enquiries, please contact:

Eckert & Ziegler AG, Karolin Riehle, Investor Relations

Robert-Rössle-Str. 10, 13125 Berlin, Germany

Tel.: +49 (0) 30 / 94 10 84-138, [email protected], www.ezag.com


2015-04-23 Dissemination of a Corporate News, transmitted by DGAP – a service of EQS Group AG.

The issuer is solely responsible for the content of this announcement.

The DGAP Distribution Services include Regulatory Announcements, Financial/Corporate News and Press Releases.

Media archive at www.dgap-medientreff.de and www.dgap.de


Language: English
Company: Eckert & Ziegler Strahlen- und Medizintechnik AG
Robert-Rössle-Str.10
13125 Berlin
Germany
Phone: 49 30 941084-138
Fax: 49 30 941084-112
E-mail: [email protected]
Internet: www.ezag.de
ISIN: DE0005659700
WKN: 565970
Listed: Regulated Market in Frankfurt (Prime Standard), Stuttgart; Regulated Unofficial Market in Berlin, Dusseldorf, Hamburg, Munich
End of News DGAP News-Service
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347429  2015-04-23

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