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DSCP > SEC Filings for DSCP > Form 10-Q on 10-Nov-2008All Recent SEC Filings

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Form 10-Q for DATASCOPE CORP


10-Nov-2008

Quarterly Report


Item 2. Management's Discussion and Analysis of Financial Condition and Results
of Operations
Business Overview
Datascope Corp. is the global leader of intra-aortic balloon counterpulsation and a diversified medical device company that develops, manufactures and markets proprietary products for clinical health care markets in interventional cardiology and radiology, cardiovascular and vascular surgery, and critical care. Our products are sold throughout the world through direct sales representatives and independent distributors. Our largest geographic markets are the United States, Europe and Japan.
We have two reportable segments, Cardiac Assist Products and Vascular Products. The Cardiac Assist Products segment accounted for 82% of total sales in fiscal 2008. The Cardiac Assist Products segment sells intra-aortic balloon pumps and catheters, endoscopic vessel harvesting products and the Safeguard™ assisted pressure device. Our intra-aortic balloon pump system is used in the treatment of cardiac shock, acute heart failure, irregular heart rhythms, and for cardiac support in open-heart surgery, coronary angioplasty, and stenting. The balloon catheter serves as the pumping device within the patient's aorta. The Vascular Products segment sells a proprietary line of knitted and woven polyester vascular grafts and patches for reconstructive vascular and cardiovascular surgery, peripheral vascular stent products and stent grafts. The peripheral vascular products are used by vascular surgeons and interventional radiologists for the treatment of peripheral arterial disease.
We believe that customers, primarily hospitals and other medical institutions, choose among competing products on the basis of product performance, features, price and service. In general, we believe price has become an important factor in hospital purchasing decisions because of pressure to cut costs. These pressures on hospitals result from Federal and state regulations that limit reimbursement for services provided to Medicare and Medicaid patients. There are also cost containment pressures on healthcare systems outside the United States, particularly in certain European countries. Many companies, some of which are substantially larger than us, are engaged in manufacturing competing products. Our products are generally not affected by economic cycles.
Our sales growth depends in part upon the successful development and marketing of new products. We continue to invest in research and development. Our growth strategy includes selective acquisitions or licensing of products and technologies from other companies.
On September 15, 2008, we entered into an Agreement and Plan of Merger (the "Merger Agreement") with Getinge AB ("Getinge") and DaVinci Merger Sub, Inc. ("Purchaser"), a wholly-owned subsidiary of Getinge, a company organized under the laws of Sweden. Subject to the terms and conditions of the Merger Agreement, Purchaser has commenced a cash tender offer (the "Offer") to purchase all of the outstanding shares of common stock of Datascope at a price of $53.00 per share. Upon completion of the tender offer and subject to the terms and conditions of the Merger Agreement, Purchaser will merge with and into Datascope, with each outstanding share of our common stock being converted into the right to receive $53.00 in cash. We will survive the merger as a wholly-owned subsidiary of Getinge.
The transaction is subject to customary conditions, including the tender of a majority of the outstanding shares of Datascope common stock into the tender offer, regulatory approvals and the absence of a material adverse change with respect to Datascope. Lawrence Saper, the Chairman of our Board of Directors, Chief Executive Officer and a 17.5% stockholder, entered into a voting agreement, dated September 15, 2008 (the "Voting Agreement") and has tendered all shares of common stock of Datascope held by him pursuant to the Offer in accordance with the terms of the Voting Agreement. According to a press release issued by Getinge on November 5, 2008, as of the close of business on November 4, 2008, approximately 13,338,318 common stock of Datascope, representing approximately 84% of the total outstanding shares of common stock of Datascope, has been validly tendered and not withdrawn in the Offer. Under the Hart-Scott-Rodino Antitrust Improvements Act of 1976, as amended (the "HSR Act"), the Offer may not be completed until the expiration of a 15-calendar day waiting period following the filing of the Notification and Report Forms
("HSR Forms") concerning the Offer with the Federal Trade Commission (the "FTC")
and the Antitrust Division of the Department of Justice, unless the waiting period is extended by a request for additional information or documentary material. Getinge originally filed its HSR Forms with the FTC on September 29, 2008, voluntarily withdrew its HSR Forms on October 14, 2008 and re-filed its HSR Forms with the FTC on October 16, 2008. On October 31, 2008, we announced that we received a Request for Additional Information from the FTC, seeking additional information concerning Getinge's proposed acquisition of Datascope. Effective May 1, 2008, we sold our Patient Monitoring ("PM") business to Mindray Medical International Limited. The sale of the PM business allows us to focus our efforts on our Cardiac Assist Products and Vascular Products segments. We received approximately $209 million in cash at the closing and retained approximately $30 million of receivables generated by the PM business.


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In October 2006, we announced a plan to exit the vascular closure market and phase out the Interventional Products ("IP") business. On August 6, 2008, we completed the sale of assets related to the VasoSeal, On-Site, and X-Site vascular closure devices, and our collagen operations, to St. Jude Medical, Inc. for $21.0 million in cash at closing and $3.0 million to be paid upon the expiration of an 18 month indemnification period. In February 2007, we completed the sale of our ProGuide™ chronic dialysis catheter and the associated assets for $3.0 million plus a royalty on future sales of the ProGuide catheter. In June 2008, we exercised our option to acquire the Peripheral Vascular Stent business of the Sorin Group of Milan. The acquisition follows our successful experience as exclusive distributor of the Sorin peripheral stent product line in Europe, during which sales have grown rapidly since the product launch in January 2007. With the acquisition, we now gain the opportunity to market the product line throughout the world. We estimate the worldwide market at $800 million annually, of which $200 million is in Europe, $500 million is in the United States and $40 million is in Japan.
Our Safeguard™ assisted pressure device received FDA 510(k) clearance to claim reduced manual compression time to stop bleeding following femoral arterial catheterization in diagnostic and interventional procedures in March 2007. In May 2007, following FDA clearance of the new clinical claim, we tripled the Safeguard sales and marketing effort in the United States from a pilot sales group to the entire Cardiac Assist direct sales force. Safeguard is aimed at an estimated $125 million annual worldwide market.
We are committed to improving our operating margins through increasing the efficiency of our manufacturing operations and cost containment programs. Due to the sale of the PM and IP businesses, which are classified as discontinued operations, the below Results of Operations relates to our continuing businesses, primarily Cardiac Assist and InterVascular. Results of Operations
Net Sales (Sales)
Sales increased $8.2 million, or 17%, in the first quarter of fiscal 2009 to $56.2 million compared to $48.0 million in the first quarter of fiscal 2008. Favorable foreign exchange translation increased sales by $1.1 million, or 2%, as a result of the weaker U.S. dollar relative to the Euro and the British Pound, the primary currencies in countries in which we have direct sales subsidiaries.
Sales increased $1.0 million, or 5%, in the United States to $22.6 million, compared to the corresponding period last year, primarily attributable to increased sales in Vascular Products ($0.6 million) and Cardiac Assist products ($0.2 million). Sales in international markets of $33.6 million increased $7.2 million or 27% compared to last year. Favorable foreign exchange translation increased international sales by $1.1 million, or 4%, due to increased sales in Cardiac Assist ($5.5 million) and Vascular products ($1.7 million).


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Cardiac Assist
Sales of Cardiac Assist products in the first quarter of fiscal 2009 increased 14% to $45.4 million, primarily reflecting continued strong sales growth in international markets for balloon pumps (41%) and intra-aortic balloons (IABs) (16%).
Sales of the Safeguard device, which grew 20% over last year, has also increased our presence in the cardiac catheterization lab and given our sales representatives additional opportunities to promote the use of IABs. Favorable foreign exchange translation contributed $0.6 million to Cardiac Assist sales in the first quarter of fiscal 2009. Vascular Products
Sales of vascular products in the first quarter of fiscal 2009 increased 29% to $10.4 million. The increase was principally due to higher worldwide sales of vascular grafts (34%) and a 16% increase in sales of peripheral vascular stent products. Increased sales of vascular grafts were attributable to higher sales to our exclusive distributor in the United States and an increase in sales to international markets (24%) as market share increased to offset continued growth of less invasive therapies and competitive pricing pressure in the European markets. Favorable foreign exchange translation contributed $0.5 million to vascular product sales in the first quarter of fiscal 2009.
Sales of Genisphere products were $0.4 million in the first quarter of fiscal 2009, compared to $0.3 million in the corresponding period last year. Gross Profit (Net Sales Less Cost of Sales) Gross profit increased $5.1 million or 16% in the first quarter of fiscal 2009 primarily as a result of increased sales in the Cardiac Assist Products segment ($5.6 million) and the Vascular Products segment ($2.6 million). Gross margin was 64.8% in the first quarter of fiscal 2009 compared to 65.2% last year. The lower gross margin percentage in the first quarter of fiscal 2009 compared to the same period last year was principally due to a less favorable mix of products as a result of increased sales of lower-margin balloon pumps to international distributors.
Research and Development Expense (R&D)
R&D expense includes new product development and improvements of existing products, as well as expenses for regulatory filings and clinical evaluations. R&D expense was $5.0 million in the first quarter of fiscal 2009, equivalent to 9.0% of sales, compared to $5.0 million or 10.3% of sales last year. R&D expense for the Cardiac Assist Products segment was $2.6 million in the first quarter of fiscal 2009 compared to $2.8 million last year, with the decrease primarily due to higher capitalization of balloon pump software development costs this year, which reduced R&D expenses compared to the prior year ($0.1 million).


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R&D expense for the Vascular Products segment was $1.3 million in the first quarter of fiscal 2009 compared to $1.1 million in the corresponding period last year, with the increase primarily attributable to increased new product development costs ($0.2 million) and unfavorable foreign currency translation
($0.1 million)
The balance of consolidated R&D is in the Corporate and Other segment and amounted to $1.1 million in fiscal 2009, unchanged compared to the corresponding period last year. Corporate and Other R&D includes corporate design, technology, regulatory and Genisphere R&D expenses.
Selling, General & Administrative Expense (SG&A) Total SG&A expense was $24.6 million in the first quarter of fiscal 2009, or 43.8% of sales, compared to $20.4 million, or 42.7% of sales.
SG&A expense for the Cardiac Assist Products segment of $19.3 million, increased $2.5 million or 15% in the first quarter of fiscal 2009 primarily attributable to increased selling and clinical expenses ($1.0 million) related to increased headcount and the AMI clinical study, higher corporate allocation ($1.0 million) and unfavorable foreign currency translation ($0.3 million). As a percentage of segment sales, SG&A expense was 42.5% in the first quarter of fiscal 2009 compared to 42.3% in the corresponding period last year.
SG&A expense for the Vascular Products segment of $6.1 million, increased $1.7 million or 37% in the first quarter of fiscal 2009 primarily attributable to unfavorable foreign currency translation ($0.5 million), increased profit sharing expense ($0.2 million) and higher corporate allocation ($0.7 million). As a percentage of segment sales, SG&A expense was 59.1% in the first quarter of fiscal 2009 compared to 55.5% in the corresponding period last year. Segment SG&A expense includes allocated corporate G&A charges. The higher corporate allocations noted above in the Cardiac Assist and Vascular Products segments were primarily attributable to increased corporate expenses for bonus ($0.7 million), the addition of a COO ($0.5 million) and increased legal fees ($0.4 million).
The weaker U.S. dollar compared to the Euro and the British Pound increased total SG&A expense by approximately $0.9 million in the first quarter of fiscal 2009.
Special Charges
In connection with Getinge AB's proposed acquisition of the Company, we incurred acquisition related expenses for legal, investment banking and other professional fees of approximately $1.5 million in the first quarter of fiscal 2009.
Interest Income
Interest income of $1.6 million in the first quarter of fiscal 2009 increased $1.0 million compared to the same period last year due to an increase in the average investment portfolio balance ($259.0 million vs. $43.9 million) partially offset by a decrease in the interest rate yield to 2.3% from 4.3%. Gain on Sale of Investment
We had a preferred stock investment of $5.0 million in Masimo Corporation, a supplier to our Patient Monitoring business. On August 13, 2007, Masimo completed its initial public offering, and concurrently,


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we sold substantially all of our investment in Masimo, resulting in a pretax gain on the sale of approximately $13.2 million in the first quarter of fiscal 2008.
Income Taxes
In the first quarter of fiscal 2009, the consolidated effective tax rate for continuing operations was 38.6% compared to 39.0% in the same period last year. The higher tax rate in the first quarter last year reflected the higher tax rate on the gain on the sale of an investment of $13.2 million. Our effective tax rate is generally impacted by changes in the geographic mix of our earnings. On October 3, 2008, the Emergency Economic Stabilization Act 2008 ("EESA") was signed into law. The EESA extended the R&D tax credit to December 31, 2009 and is retroactive to January 1, 2008. Our effective tax rate for the first quarter of fiscal 2009 does not reflect the benefit of the R&D tax credit for fiscal 2009 nor the favorable impact of the retroactive provisions of the EESA to January 1, 2008 because the new law was passed after the end of the first quarter of fiscal 2009.
Net Earnings from Continuing Operations
Net earnings from continuing operations were $4.0 million, or $0.25 per diluted share, in the first quarter of fiscal 2009 compared to $11.9 million, or $0.76 per diluted share, in the first quarter of fiscal 2008. The lower earnings in the first quarter of fiscal 2009 was primarily attributable to the after-tax gain on sale of investment of $6.5 million in the first quarter last year. Net Loss from Discontinued Operations
Net loss from discontinued operations of the PM and IP businesses was $1.7 million in the first quarter of fiscal 2009, and $0.1 million in the same period last year with the increased loss primarily attributable to lower sales in the first quarter of fiscal 2009.
Gain on sale of Discontinued Operations
In the first quarter of fiscal 2009, we recognized a gain on sale of the IP business of $0.6 million, net of tax.
Liquidity and Capital Resources
We consider our cash and cash equivalents, short-term investments and our available unsecured lines of credit to be our principal sources of liquidity. Cash and cash equivalents and short-term investments at September 30, 2008 were $243.3 million compared to $250.2 million at June 30, 2008. Long-term investments were $23.0 million and $22.8 million at September 30, 2008 and June 30, 2008, respectively. Working capital was $291.4 million at September 30, 2008 compared to $279.2 million at June 30, 2008, and the current ratio was 6.5:1 compared to 4.0:1 at the end of fiscal 2008.
The increase in working capital and the current ratio was primarily due to an increase in cash and cash equivalents ($168.2 million) and a decrease in income taxes payable ($33.4 million), partially offset by a decrease in short-term investments ($175.1 million) and accounts receivable ($16.0 million).


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The increase in cash and cash equivalents and the decrease in short-term investments was primarily due to investing the proceeds from a matured Treasury bill into a United States Government money market mutual fund at the end of September 2008.
From a cash and short-term investments perspective, we remain primarily invested in highly-liquid and highly-rated securities, including U.S. treasury securities, U.S. government agency securities, Foreign government treasury securities, and Guaranteed foreign current deposits.
The decrease in accounts receivable was principally due to the lower sales and continued collection of the $30.0 million of PM accounts receivable. In the first quarter of fiscal 2009, we used $24.3 million of net cash in our operating activities compared to $9.2 million of cash provided from operating activities in the first quarter of the prior year. The decrease in cash provided by operations in the first quarter of fiscal 2009 was primarily attributable to a reduction in income taxes payable as a result of the payment of taxes related to the gain on sale of the PM business in the fourth quarter last year. In the first quarter of fiscal 2009, we provided a net $191.4 million of cash from investing activities. Net sales and maturities of investments yielded $178.3 million and proceeds from the sale of the IP business added $21.0 million of cash. These $199.3 million of proceeds were spent on $3.5 million of investment purchases, $3.6 million of capital expenditures and technology and $0.6 million of capitalized software.
In the first quarter of fiscal 2009, we provided a net $3.1 million of cash from financing activities, primarily from $2.9 million of proceeds from the exercise of stock options and $0.3 million of excess tax benefits to be realized from stock-based awards.
At September 30, 2008, we had available unsecured lines of credit totaling approximately $101.0 million, with interest payable at LIBOR-based rates, determined by the borrowing period. Of the total available, $25.0 million expires in October 2008 and $50.0 million expires in March 2009. We also have $26.0 million in credit lines with no expiration date. These lines of credit are renewable annually at the option of the banks. The $25.0 million credit line that expired in October 2008 was not renewed by the bank. We plan to seek renewal of all other lines of credit.
We purchased approximately 2,500 shares of our common stock during the first quarter of fiscal year 2009. We have a remaining balance of $1.0 million available under the stock repurchase program authorized by the Board of Directors on May 16, 2001. Due to the pending merger, we do not plan on repurchasing additional shares of our common stock during the remainder of fiscal 2009.
On September 15, 2006, the Board of Directors approved an additional stock repurchase program for $40 million of our common stock. Purchases under this program may be made from time to time on the open market or in privately negotiated transactions, and may be discontinued at any time at the discretion of the Company.
On September 16, 2008, the Board of Directors declared a quarterly cash dividend of $0.10 per share, which was paid on October 15, 2008 to stockholders of record as of October 1, 2008.
We believe that our existing cash and investment balances, future cash generated from operations and existing credit facilities will be sufficient to meet our projected working capital, capital and investment needs. The moderate rate of current United States and European inflation has not significantly affected the Company.


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Subsequent Event
On October 15, 2008, we transferred approximately $45.2 million to a Grantor Trust ("Trust") to provide for amounts which may become payable in the future to certain of our executives pursuant to various employment, supplemental benefit and severance agreements upon a change of control of the Company. The funding of the Trust was required as a result of the Merger Agreement entered into on September 15, 2008, providing for the acquisition by Getinge of all of the outstanding shares of our common stock for $53.00 per share Information Concerning Forward Looking Statements The statements in this Management's Discussion and Analysis of Financial Condition and Results of Operations that are not strictly historical are "forward-looking" statements within the meaning of the Private Securities Litigation Reform Act of 1995 and are intended to be covered by the safe harbors provided therein. Forward-looking statements involve risks and uncertainties that could cause actual results to differ materially from those projected in the forward-looking statements. Many of these risks cannot be predicted or quantified and are at least partly outside our control. The forward-looking statements included in this press release are made only as of the date of this report and the Company undertakes no obligation to update these forward-looking statements to reflect subsequent events or circumstances. Critical Accounting Policies
Our financial statements have been prepared in accordance with accounting principles generally accepted in the United States of America. The preparation of these financial statements requires us to make estimates and assumptions that affect the reported amount of assets and liabilities and disclosure of contingent assets and liabilities at the date of the financial statements and the reported amount of revenues and expenses for each period. We regularly evaluate our estimates and assumptions on an on-going basis and adjust as necessary to accurately reflect current conditions. These estimates and assumptions are based on current and historical experience, on information from third party professionals and on various other factors that are believed to be reasonable under the circumstances. Actual results could differ from those estimates. Our critical accounting policies include Revenue Recognition, Allowance for Doubtful Accounts, Inventory Valuation, Income Taxes and Pension Plan Actuarial Assumptions, as disclosed in our Form 10-K for the fiscal year ended June 30, 2008.
Recent Accounting Pronouncements
On July 1, 2008, we adopted the provisions of the Financial Accounting Standards Board ("FASB") Emerging Issues Task Force Issue No. 06-10, Accounting for Deferred Compensation and Postretirement Benefits Aspects of Collateral Assignment Split-Dollar Life Insurance Arrangements. The Task Force concluded that an employer should recognize a liability for the postretirement benefit related to a collateral assignment split-dollar life insurance arrangement in accordance with either FASB Statement No. 106, Employers' Accounting for Postretirement Benefits Other Than Pensions, or Accounting Principles Board Opinion No. 12, Omnibus Opinion, based on the substantive agreement with the employee. The Task Force also concluded that an employer should recognize and measure an asset based on the nature and substance of the collateral assignment split-dollar life insurance arrangement. The Supplemental Benefits Plan for the Chairman and Chief Executive Officer, Mr. Lawrence Saper, provides survivor benefits in the form of a $10 million life insurance policy, maintained pursuant to a collateral assignment split-dollar agreement among Mr. Saper, the Company and a trust for the benefit of Mr. Saper's family. At adoption date, we recognized a $3.5 million noncurrent liability for the present value of the premium reimbursement through a cumulative effect adjustment to retained earnings. The noncurrent liability is reflected in other liabilities in our condensed consolidated balance sheet.


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In September 2006, the FASB issued SFAS No. 157, Fair Value Measurements ("SFAS 157"). SFAS 157 defines "fair value" as: the price that would be received to sell an asset or paid to transfer a liability in an orderly transaction between market participants at the measurement date. In addition, SFAS 157 establishes a fair value hierarchy to be used to classify the source of information used in fair value measurements, new disclosures of assets and liabilities measured at fair value based on their level in the hierarchy and a modification of the long-standing accounting presumption that the transaction price of an asset or liability equals its initial fair value. In February 2008, the FASB issued Staff Position FAS 157-2, Effective Date of FASB Statement No. 157, which delayed the provisions of SFAS 157 relating to nonfinancial assets and liabilities until fiscal years beginning after November 15, 2008 (our fiscal year 2010 beginning July 1, 2009). Accordingly, we adopted the required provisions of SFAS 157 at the beginning of our fiscal 2009 (July 1, 2008) and the remaining provisions will be adopted at the beginning of our fiscal 2010. The fiscal 2009 adoption did not result in a material impact to our consolidated financial statements, but it did result in certain additional disclosures. We are currently evaluating the impact of adopting the remaining parts of SFAS 157 on our consolidated financial statements. See Note 12 for additional information (disclosure) related to the impact of adopting SFAS 157.
In February 2007, the FASB issued SFAS No. 159, The Fair Value Option for Financial Assets and Financial Liabilities - Including an amendment of FASB Statement No. 115 ("SFAS 159"). This statement provides an option to report selected financial assets and liabilities at fair value. In addition, SFAS 159 establishes presentation and disclosure requirements for those assets and liabilities which the registrant has chosen to measure at fair value. SFAS 159 is effective for fiscal years beginning after November 15, 2007 (our fiscal year 2009 beginning July 1, 2008). We have not elected the fair value option for eligible items that existed at the beginning of our fiscal 2009. In December 2007, the FASB issued SFAS No. 160, ("SFAS 160") Noncontrolling Interests in Consolidated Financial Statements - an amendment of ARB No. 51. This statement amends ARB 51 to establish accounting and reporting standards for the noncontrolling interest in a subsidiary and for the deconsolidation of a . . .

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