OMER, Israel, Aug. 01, 2018 (GLOBE NEWSWIRE) -- Medigus Ltd. (NASDAQ: MDGS) (TASE: MDGS), a medical device company
developing minimally invasive endosurgical tools and an innovator in direct visualization technology, today announced an exclusive
distribution agreement for its Medigus Ultrasonic Surgical Endostapler (MUSE™) system in the U.S. with Micro-Tech Endoscopy
USA, Inc., a leading global manufacturer of GI endoscopy disposables and non-vascular stents, and wholly – owned subsidiary of
Micro-Tech (Nanjing) Co. Ltd. The new commercialization agreement takes effect immediately for an initial term of three years with
annual increases in minimum purchases for the first seven years. Medigus also has an exclusive distribution agreement with
Micro-Tech Europe for the MUSE™ system in Germany.
The MUSE™ procedure, currently covered under a CMS Category I CPT® Code of 43210 for Transoral Fundoplication
(TF) procedures, took effect in 2016, with updated coding and payment information posted by the Federal Register in January of
2018. This update, which includes a 93% facility payment increase over the prior APC classification, will benefit the U.S. launch
of the MUSE™ system from a reimbursement standpoint.
“This agreement is consistent with our strategy to commercialize our innovative products in targeted markets,”
said Chris Rowland, CEO of Medigus. “Medigus is pleased to add Micro-Tech Endoscopy USA, Inc. to our distribution team, and are
looking forward to broadening MUSE™ availability through its very capable U.S. sales organization. This agreement is an organic
extension of the strong relationship we already have with Micro-Tech Europe - we are delighted that Micro-Tech recognizes the
quality and innovation of our products.”
“We look forward to offering our customers Medigus’ outstanding product solutions,” said Chris Li, President of
Micro-Tech Endoscopy USA. “The addition of MUSE™ to our growing portfolio supports our goal of arming our team with cutting-edge
products that provide better outcomes and value to healthcare providers and patients.”
The MUSE™ system is a single-use flexible transoral stapler that merges the latest advancements in microvisual,
ultrasonic and surgical stapling. The device comes equipped with an ultrasonic sight and range finder and a micro ScoutCam™ CMOS
camera, which enables a single physician to perform an incisionless transoral fundoplication – the procedure intended to treat the
anatomical cause of GERD, commonly referred to as acid reflux.
Those who experience symptoms such as heartburn or regurgitation twice a week or more, may be at risk for
persistent GERD.
For more information, please visit www.medigus.com or www.RefluxHelp.com.
About Medigus
Medigus is a medical device company specializing in developing minimally invasive endosurgical tools and highly innovative imaging
solutions. Medigus is the pioneer developer of the MUSE™ system, an FDA cleared and CE marked endoscopic device to perform
Transoral Fundoplication (TF) for the treatment of GERD (gastroesophageal reflux disease), one of the most common chronic
conditions in the world. In 2016, the CMS established the Category I CPT® Code of 43210 for TF procedures, such as the ones
performed with MUSE, which establishes reimbursement values for physicians and hospitals. Medigus makes persistent efforts to gain
MUSE adoption in key markets around the world – it is available in world-leading healthcare institutions in the U.S., Europe and
Israel. Medigus is also in the process of obtaining regulatory clearance in China. Medigus is traded on the Nasdaq Capital Market
and the TASE (Tel-Aviv Stock Exchange Ltd.). To learn more about the company’s advanced technology, please visit www.medigus.com or
www.RefluxHelp.com.
About Micro-Tech Endoscopy USA
Micro-Tech is a leading global manufacturer of GI endoscopy disposables (biopsy forceps, snares, injection needles, hemoclips,
balloons and other accessories) and non-vascular stents. Established in 2000 in Nanjing, China, Micro-Tech manufactures and sells
its products to healthcare providers throughout the world. In 2015, Micro-Tech entered the US market and quickly grew its customer
base offering exceptional solutions and innovative technologies such as the SureClip®. To learn more about the
company, please visit www.mtendoscopy.com.
This press release may contain statements that are “Forward-Looking Statements,” which are based upon the
current estimates, assumptions and expectations of the company’s management and its knowledge of the relevant market. The company
has tried, where possible, to identify such information and statements by using words such as “anticipate,” “believe,” “envision,”
“estimate,” “expect,” “intend,” “may,” “plan,” “predict,” “project,” “target,” “potential,” “will,” “would,” “could,” “should,”
“continue,” “contemplate” and other similar expressions and derivations thereof in connection with any discussion of future events,
trends or prospects or future operating or financial performance, although not all forward-looking statements contain these
identifying words. These forward-looking statements represent Medigus’ expectations or beliefs concerning future events, and
it is possible that the results described in this press release will not be achieved. By their nature, Forward-Looking Statements
involve known and unknown risks, uncertainties and other factors which may cause future results of the company’s activity to differ
significantly from the content and implications of such statements. Other risk factors affecting the company are discussed in
detail in the company's filings with the Securities and Exchange Commission. Forward-Looking Statements are pertinent only as of
the date on which they are made, and the company undertakes no obligation to update or revise any Forward-Looking Statements,
whether as a result of new information, future developments or otherwise. Neither the company nor its shareholders, officers and
employees, shall be liable for any action and the results of any action taken by any person based on the information contained
herein, including without limitation the purchase or sale of company securities. Nothing in this press release should be deemed to
be medical or other advice of any kind.
MEDIA CONTACT:
John Guerriero
Lazar Partners Ltd.
646-871-8492
jguerriero@lazarpartners.com