Liam Kelly
Analyst · Raymond James. Your line is now open
Thank you, Benson and good morning everyone. For the consolidated company, first quarter 2016 constant currency revenue grew 1.1%. If you were to normalize our first quarter results for the two fewer shipping days, our constant currency revenue growth would have been approximately 3.3%. As mentioned earlier, we faced a tough comparable in Q1 2015 where if you recall, we grew by 5.2% with one less shipping day. This comparable eases in quarter two and three, in addition we will have one additional shipping day in quarter two and another in quarter four. As such, we expect to see a strengthening in sales growth beginning in quarter two, and although this phasing may be lumpy, this is consistent with our internal expectations on revenue for the quarter and year. Sales of new products introduced to the market contributed 1.1% and were the main driver of revenue growth in the quarter. New product sales were particularly strong within our Surgical and OEM businesses, as well as within our EMEA segment. And while not yet a key contributor in terms of revenue dollars, we continue to make progress in two key strategic initiatives, the launch of Percuvance within our Surgical business, and the LMA Protector within our Anesthesia business. First to Percuvance; the recent stage of meeting in Boston was an important event signaling our upcoming full market release. Clinician feedback continues to reinforce what we learned in our limited market release, which that Percuvance is equal to standard 5 millimeter laparoscopic instruments in terms of rigidity, so causing less trauma to the patient with virtually scarless incisions. The strength and functionality of the 5 millimeter end effector is a exceeding our initial expectations, even during complex cases with challenging patient anatomy. We recently completed the first cases with our second generation Percuvance device in Europe, where we are currently in full market release, having received a CE mark in quarter one, while within the US, we are currently selling our first generation Percuvance device and are working with the FDA to get our second generation device 510(k) approved. The FDA recently informed us that we will need to do a sterilization study and update the instructions for use, prior to commercialization of the second generation product within the US. And as such, it is our belief that we will be in a position to do a full market release of our second generation Percuvance products offering in early Q3. We do not expect this to have a negative impact on 2016 revenues, as we will continue to demonstrate and sell the first generation product. Next to the LMA Protector; we have registrations in places from most major markets, and continue with our controlled market rollout with an anticipated full market release in 2017. The Protector is currently being evaluated in 40 hospitals around the world, as part of this rollout. This compares to only 11 hospitals, when I last spoke to you on our February conference call. Clinical feedback has been very positive as the design is getting high marks for its seal pressure, which is a critical component to protecting the airway and facilitating ventilation. I am pleased with the status of both of these product launches and I continue to believe that both are large, multi-year opportunities for Teleflex. Turning to other components of revenue growth; previously completed acquisitions and distributor conversions continue to pay a benefit, and during the quarter added approximately 70 basis points of growth, which was primarily due to the acquisitions of Stenning, Human Medics, and Trintris. Moving to core product pricing; during quarter one, we saw the average selling price of our products expand approximately 20 basis points. This was primarily due to increases in surgical and vascular access, somewhat offset by a decline in European product pricing. Finally, during the quarter, sales volume of existing products declined by approximately 90 basis points. This was primarily the result of two fewer shipping days in the quarter, as well as the impact of destocking by our large US distributors. The sales [tracking] from these distributors show positive sales volume at a hospital level. In addition as Benson said a few moments ago, we also had some of the OEM customers push out orders to the second quarter, and in North America we saw an anemic flu season, which principally affected some of our respiratory therapy and CVC products. Next, I would like to provide some additional color surrounding our segment and product related constant currency revenue growth drivers. Vascular North America first quarter revenue increased 1.5% to $81.5 million. The increase in vascular revenue was largely due to the sales of Vidacare, EZ-IO and OnControl devices. Now to Anesthesia North America; first quarter revenue was $46 million, up 1.6% versus the prior year period. Growth in this segment was driven by increased sales of Vidacare, EZ-IO and airway management devices, somewhat offset by lower sales of regional anesthesia product offerings. Turning to our Surgical North America business, its revenue increased 3.1% to $38.9 million. The increase within surgical is attributable to higher sales of chest drainage and Mini-Lap products. Shifting to our overseas businesses, EMEA revenues declined on a constant currency revenue basis by 1.9% and totaled $122.1 million. The decline in European revenue was the result of the shipping day impact and a reduction in some products’ pricing. Moving to Asia, our first quarter revenue increased 6.4% to $49.2 million. The quarterly increase in Asia revenue was primarily due to higher surgical ligation and central venous catheter sales, and the positive impact from the acquisitions of Stenning and Human Medics. Now to OEM; revenue in the first quarter decreased 1.6% to $34 million, almost primarily due to lower sales of catheter and extrusion products, as well as the previously mentioned order movement from quarter one to quarter two. This was somewhat offset by an increase in performance fiber sales. Given the underlying business trend, it is our firm expectation that OEM sales will rebound nicely during quarter two. Lastly, first quarter revenues for the businesses within our all other category was up 2.6%, totaling $53.2 million. Growth here is primarily attributable to sales of the additional cardiac intra-aortic balloon products. This was somewhat offset by lower sales within Latin American markets, due to the macroeconomic issues facing those countries. Finally before I turn the call over to Tom, I would like to update you on additional group purchasing organization and IDN agreements that we received during the quarter. Building on our success in 2015, during the first quarter we won 12 new agreements and extended another 20. This quarterly total surpasses what we achieved in the fourth quarter of 2015 and now represents the largest number of agreements awarded in any single quarter since we became a pure play medical device company. As you will continue to hear me say, these relationships are extremely important to us, as they bolster our ability to continue to drive volume growth across our product portfolio. Of the agreements won in quarter one several were Sole Source Award. That takes me to the end of my prepared remarks. At this time, I would like to turn the call over to Tom for him to review our financial results for the first quarter and our 2016 guidance. Tom?