Liam Kelly
Analyst · David Lewis from Morgan Stanley. Please go ahead
Thank you, Benson, and good morning everyone. For the consolidated company, second quarter 2015 constant currency revenues grew 4.7% and similar to the first quarter the revenue growth was broad-based both in terms of product lines and geographic regions. The major drivers of revenue growth this quarter came from improved sales volumes of approximately 262 basis points of revenue growth. This growth was driven by core product growth of 215 basis points, and Vidacare growth of 47 basis points. Vidacare product sales grew approximately 11% on a constant currency basis as compared with the prior year period. While this was good, it was lower than the growth we generated in the first quarter of 2015. The revenue growth rate of Vidacare product sales in the second quarter was down sequentially due to seasonality of military sales, and the timing of some crash car sales that occurred in the first quarter of this year. We continued to achieve approximately 30% revenue growth in the interventional products globally and nearly 20% growth in the EZ-IO products in Europe. During the quarter we also had our first Italian ambulance conversion. We continue to invest aggressively behind Vidacare and we remain extremely bullish on the product's potential. In fact, we expect Vidacare revenues to grow approximately 20% on a constant currency basis for the remainder of 2015. Turning to core product volumes, the increase this quarter was led by improved Vascular, OEM, and Respiratory sales for a domestic perspective. Our CVC business grew approximately 10% globally in the quarter driven by market share gains and product upgrades in the U.S., Europe, and Latin America, and volume gains in Asia-Pacific. While from an international standpoint, core product volume growth was great in Asia, thanks to additional orders coming from China, as well as increased sales in Japan. During the quarter, we also experienced strong core product volume increases throughout Europe, as well as in Latin American markets. Another contributor to our revenue growth this quarter was the continued penetration of new products in the market place. During the second quarter, new product introductions contributed approximately 89 basis points of revenue growth. This was led by sales of our European EASK CVC kits, surgical product introduction stemming from our partnership with a robotics provider, sales of our AutoFuser Disposable Pain Pump, and sales of our Rusch Disposable LED Laryngoscope. Additional sales coming from new product introductions in the quarter were somewhat offset by a decline in new products sales within our vascular business. This was due to the product recall issue which Benson mentioned earlier, as it impacted sales of our ArrowADVANTAGE5 preloaded PICC. We expect new product sales within our vascular segment to rebound during the remainder of the year. Excluding this recall, constant currency revenue growth for the company coming from new product sales would have exceeded 100 basis points. Turning to pricing. During the second quarter the average selling price of our core products were flat as compared with the prior year period. Similar to recent quarters we were able to achieve price increases within our North American surgical business. However, this was offset by price pressures primarily coming from European markets. And finally, this takes me to the last component of quarterly revenue growth or the contribution we received from M&A and distributor-to-direct conversions. Revenue growth from these totaled approximately 114 basis points and was primarily due to the impact of distributor conversion. The performance in this area was consistent with that achieved in the first quarter of the year. It is important to understand that as we progress through the remainder of the year, we continue to expect the contribution to revenue growth from M&A and distributor conversions to accelerate. Next, I would like to provide some additional color surrounding our segment and product related constant currency revenue growth drivers. Vascular North America second quarter revenue increased 5.6% to $81.2 million. The increase in vascular revenue was largely due to greater sales of Central Venous Catheters, Vidacare EZ-IO devices, and catheter navigation products. Moving to Anesthesia North America. Second quarter revenue was $45.6 million or flat versus the prior year period. Growth in this segment during the quarter was achieved in our LMA MAD Nasal atomization product offering. However, this was offset by the discontinuation of some third-party distribution agreements which was approximately 1%, lower sales in some of our region Anesthesia products, and lower domestic sales of laryngeal mask. And speaking of MAD Nasal, we recently received regulatory approval to expand our indication for use from a CE MAD perspective to include emergent, urgent, and medically necessary situations and when intravenous or intramuscular access may be difficult or impossible. Turning to our surgical North America business, its revenue increased 7.8% to $40.5 million. The increase in surgical revenue was due to higher sales of chest drainage, ligation clips, access boards, and Mini-Lap products. This was somewhat offset by lower sales of general surgical instruments and suture products. EMEA revenues totaled $129.1 million in the quarter and generated consistent currency revenue growth of 1.7%. This was consistent with the performance this segment realized in the first quarter and we continue to see the European market as being stable, with the increase in revenue this quarter, primarily due to higher sales of vascular products, including Vidacare and PICCs, higher sales of laryngeal masks, and increased dialysis access product sales. Moving to Asia, our second quarter revenue increased 9.4% to $62.1 million. The quarterly increase in Asia revenue was primarily due to stronger sales in China, go-direct efforts in Japan, and additional revenues in Korea due to the acquisition of Human Medics. Now to OEM. Revenues in the second quarter increased 7.5% to $37.9 million. The increase in OEM revenue was primarily due to higher sales of catheter products. And lastly, our all other segment revenue for the quarter was up 6%, totaling $55.7 million. The increase in other revenues was largely due to higher sales within Latin American countries and intra-aortic balloon pumps and catheters. Next I would like to update you on additional group purchasing and IDN agreements that we received in the quarter. In a similar fashion to the first quarter of the year, during Quarter 2, we once again won a total of 10 agreements. Of these agreements, four were brand new, while six were renewals of existing awards. One of the new GPO wins was for our Pleur-evac chest drainage products that Benson referred to earlier. The rest spanned across our product offerings that included items such as CVC and arterial access devices, intra-aortic balloon products, dialysis access and vascular positioning systems, and a brand new award for an AutoFuser disposable pain pumps. We continue to be quite pleased with the progress we are making in these areas. Next, I would like to update you on some recent product regulatory approvals that we received, as well as the findings from some independent studies that were performed in which our products were used. During the second quarter, we received 510(k) market clearance from the FDA for our Arrow Endurance Extended Dwell Peripheral Catheter System. Endurance was one of the products that we highlighted at our recent Investor Day event. This device is a single use peripheral catheter system intended for short-term dwell use to permit delivery of infusion therapy, pressure monitoring, high pressure injection, and the withdrawal of blood. The insertion device consists of an ergonomically designed handle with an integral echogenic needle. The needle has a passably active production mechanism, guide wire, release tab, and single-lumen catheter. The insertion device is designed as a closed system intended to contain blood throughout the catheter insertion process. The concept behind the Arrow Endurance system is that it will be used when a PICC may be too much for patient, but yes a peripheral IV device is not enough to solve their needs. It is our belief that through the innovative insertion design of this product that we can target a portion of peripheral IV market and turn that usage over to Endurance. We are quite excited about this product's opportunity and tend to launch it in the United States later this year. Another area of focus at the recent Investor Day surrounds our leadership position within the area of antimicrobial and anti-thrombogenic coating and helping hospitals minimize the cost associated with hospital acquired infection. Recently our Arrow Central Venous Catheters with ARROWg+ard Blue technology were included in a peer review retrospective study. The study further documented the ability of our Central Venous Catheter with ARROWg+ard Blue technology to prevent catheter related blood stream infections therefore reducing their occurrence and reducing direct cost associated with treating those infections. The antimicrobial catheter outperformed an unprotected CVC in both infection prevention and total cost per patients. Within this study, the ARROWg+ard Blue catheter achieved a zero infection rate per 1000 catheter days. In contrast, the unprotected device was associated with a higher catheter related blood stream infection rate. In addition to superior clinical performance the ARROWg+ard Blue CVC had sharply lower CVC related costs than those associated with an unprotected catheter. This study is further evident that using an unprotected catheter may put both the patient and hospitals bottom-line at unnecessary risk. And before I review two recently completed acquisitions, I would like to provide an update on the status of the LMA Protector and Percuvance product launches. The LMA Protector is the device that we've been working on which we expect would bridge the remaining gap with ET tubes and open up a large number of additional procedures both in the pre-hospital and hospital settings to LMA use. This is important to Teleflex as the margin mix benefit that would get from the migration from ET tubes to LMA use is significant. The protector has a flexible but fixed curb tubes that allows ease with surgeons and anatomical conformity. It's patented dual gastric drainage channel and chamber is designed to improve the laryngeal seal during high volume regurgitation. It also has an integrated suction fore that can be used to rapidly remove any gastric content in the patient or to regurgitate during a procedure. The protector is currently being evaluated in 22 hospitals around the world as part of a small controlled limited market release. Feedback from these controlled releases has been overwhelmingly positive. The protector design is getting high marks for its seal pressure which is a critical component to protecting the airway and facilitating ventilation. In addition, the protector silicon design and flexible curb has been well received in terms of ease of insertion. Users have also reported high praise for the advanced gastric access feature. We are quite enthusiastic about this product and it is our belief that the protector can move Teleflex forward exponentially in our quest to provide physicians with technology that reduces the risk of area-related complications. We expect a full market release in the first quarter of 2016. Now to Percuvance. As a remainder it is our belief that Percuvance has a potential to eliminate scaring and pain and improve a patient's recovery when compared to a traditional multi-port laparoscopic surgery. This device eliminates the need for multiple trocars and allows the surgeon to potentially access the surgical site with better angle. The unique feature of Percuvance allows the surgeon to use similar size operating tip. The same size they have been accustomed to using the traditional 5 millimeter, 10 millimeter straight stick laparoscopic devices without the need for a trocar. The Percuvance surgical system was first used at the Cleveland Clinic in March of this year. I am pleased to tell you that since the initial launch in March, we are currently testing the product in nine hospitals worldwide today, and anticipate that we will have the device in 17 hospitals by the end of the year. Similar to the other main protector, I am happy to report that initial feedback on Percuvance has also been extremely positive. Our key findings from the limited market release are three folds. First, it has the applicability in a broader range of procedures. Second, it has applicability in more complex procedures than first envisioned. And third, the Percuvance system has a fast deduction rate as it does not require a change in surgical practice. Next, I would like to briefly discuss two small acquisitions that were recently completed. The first was the acquisition of N. Stenning & Co. Stenning has been a distributor of Teleflex surgical products in Australia under the Pilling and Weck brand for nearly 35 years. Included in this transaction as a Stenning surgical customer relationships throughout Australia and a team of surgical sales representatives were now employees of Teleflex. This acquisition is yet another example of Teleflex executing upon its strategy of converting select distributors to a direct sales model, enabling the company to leverage our sales performance to support growth and capture additional margin. These all cash acquisition was completed in June and is expected to be modestly accretive in 2015. And lastly, I would like to touch on another acquisition that will benefit our Anesthesia segment. Completed on the first day of the third quarter was the acquisition of exclusive North American distribution rights to the AutoFuser and the AutoFuser with AutoSelector range of disposable pain control pumps from Ace Medical U.S. In connection with this transaction, Teleflex entered into a 10-year exclusive distribution agreement with the manufacturer of these products Ace Medical Corporation. This transaction solidifies Teleflex's position as a leading source of high quality regional Anesthesia products, including catheters and pain pump systems and provides the immediate benefit of a strengthening our Anesthesia business in the United States and supports our margin expansion initiatives. This too was an all cash transaction and it is also expected to be modestly accretive to revenues and earnings in 2015. That completes my prepared remarks. With that, I would like to turn the call over to Tom. Tom?