Organization, Consolidation and Presentation of Financial Statements Disclosure and Significant Accounting Policies [Text Block] | 2. Summary of Significant Accounting Policies Recently Issued Accounting Standards In January 2017, 2017 04 Simplifying the Test for Goodwill Impairment 2 December 15, 2019. January 1, 2017. not 2017 04 In February 2016, 2016 02, “Leases (Topic 842 2016 02 2016 02 December 15, 2018 not 2016 02 Recently Adopted Accounting Standards In July 2017, No. 2017 11, Earnings Per Share (Topic 260 480 815 2017 11 may no 2017 11 December 15, 2018, 2017 11 2017 11 April 1, 2018. April 1, 2018, not not April 16, 2018, 2017 11 4 Sequencing Policy Under ASC 815 40 35, 815 first 815, not On January 1, 2018, No. 2014 09, Revenue from Contracts with Customers (Topic 606 not January 1, 2018. January 1, 2018 No. 2014 09, not 605 $79,000 January 1, 2018 606, 606 Revenue Recognition Revenue is recognized based on the five 606: Step 1 Step 2 not Step 3 Step 4 one Step 5 Disaggregation of Revenue The Company’s primary revenue streams include device sales, service revenue from device maintenance contracts and clinical services. Device Sales Device sales include devices and consumables for BioArchive, AXP ®, X not Service Revenue Service revenue consists primarily of maintenance contracts for BioArchive, AXP and X one two X one three not Clinical Services Service revenue in our Clinical Development Segment includes point of care procedures and cord blood processing and storage in our clinical segment. Point of care procedures are recognized when the procedures are performed. Cord blood processing and storage is recognized as the performance obligations are satisfied. Processing revenue is recognized when that performance obligation is completed immediately after the baby’s birth, with storage revenue recorded as deferred revenue and recognized ratably over time for up to 21 June 30, 2018, $269,000 may The following table summarizes the revenues of the Company’s reportable segments for the three six June 30, 2018: Three Months Ended June 30, 2018 Device Revenue Service Revenue Other Revenue Total Revenue Device Segment: AXP $ 879,000 $ 66,000 $ -- $ 945,000 BioArchive 449,000 311,000 -- 760,000 Manual Disposables 229,000 -- -- 229,000 Other 8,000 -- 16,000 24,000 Total Device Segment 1,565,000 377,000 16,000 1,958,000 Clinical Development Segment: Manual Disposables 1,000 -- -- 1,000 Bone Marrow -- 38,000 -- 38,000 Other -- 7,000 -- 7,000 Total Clinical Development 1,000 45,000 -- 46,000 Total $ 1,566,000 $ 422,000 $ 16,000 $ 2,004,000 Six Months Ended June 30, 2018 Device Revenue Service Revenue Other Revenue Total Revenue Device Segment: AXP $ 1,564,000 $ 131,000 $ -- $ 1,695,000 BioArchive 872,000 655,000 -- 1,527,000 Manual Disposables 462,000 -- -- 462,000 Other 46,000 -- 33,000 79,000 Total Device Segment 2,944,000 786,000 33,000 3,763,000 Clinical Development Segment: Manual Disposables 23,000 -- -- 23,000 Bone Marrow -- 61,000 -- 61,000 Other -- 24,000 -- 24,000 Total Clinical Development 23,000 85,000 -- 108,000 Total $ 2,967,000 $ 871,000 $ 33,000 $ 3,871,000 Performance Obligations There is no no not may not Payments from domestic customers are normally due in two may 120 no Contract Balances The Company records a receivable when the titles of goods have transferred, maintenance contracts have been fully executed or when services have been rendered. Generally, all sales are contract sales (with either an underlying contract or purchase order). The Company does not $207,000. $384,000 $718,000 six June 30, 2018 Backlog of Remaining Customer Performance Obligations The following table includes revenue expected to be recognized and recorded as sales in the future from the backlog of performance obligations that are unsatisfied (or partially unsatisfied) at the end of the reporting period. Remainder of 2018 2019 2020 2021 and beyond Total Service revenue $ 749,000 $ 683,000 $ 209,000 $ -- $ 1,641,000 Clinical revenue 7,000 15,000 15,000 232,000 269,000 Total $ 756,000 $ 698,000 $ 224,000 $ 232,000 $ 1,910,000 Revenues are net of normal discounts. Shipping and handling fees billed to customers are included in net revenues, while the related costs are included in cost of revenues. Goodwill, Intangible Assets and Im pairment Assessments For goodwill and indefinite-lived intangible assets (clinical protocols), the carrying amounts are periodically reviewed for impairment (at least annually) and whenever events or changes in circumstances indicate that the carrying value of these assets may not ASC) 350, not 50 2 In the second 2018, June 30, 2018 3 The Company recorded an impairment charge of $12,695,000 $14,507,000 June 30, 2018, Intangible Assets Goodwill Balance at December 31, 2017, net $ 21,629,000 $ 13,976,000 Amortization and foreign exchange (current year) (83,000 ) -- Impairment loss (14,507,000 ) (12,695,000 ) Balance at June 30, 2018, net $ 7,039,000 $ 1,281,000 Fair Value Measurements In accordance with ASC 820, Fair Value Measurements and Disclosures The guidance also establishes a hierarchy for inputs used in measuring fair value that maximizes the use of observable inputs and minimizes the use of unobservable inputs by requiring that the most observable inputs be used when available. Observable inputs are inputs that market participants would use in valuing the asset or liability and are developed based on market data obtained from sources independent of the Company. Unobservable inputs are inputs that reflect the Company’s assumptions about the factors that market participants would use in valuing the asset or liability. The guidance establishes three may Level 1: Level 2: Level 3: The carrying values of cash and cash equivalents, accounts receivable and accounts payable approximate fair value due to their short duration. The fair value of the Company’s derivative obligation liability is classified as Level 3 Segment Reporting Operating segments are defined as components of an enterprise about which separate financial information is available that is evaluated regularly by the Chief Operating Decision Maker (CODM), or decision making group, whose function is to allocate resources to and assess the performance of the operating segments. The Company has identified its chief executive officer and chief operating officer as the CODM. In determining its reportable segments, the Company considered the markets and the products or services provided to those markets. The Company has two ● The Clinical Development Division, is developing autologous (utilizing the patient’s own cells) stem cell-based therapeutics that address significant unmet medical needs for applications within the vascular, cardiology and orthopedic markets. ● The Device Division, engages in the development and commercialization of automated technologies for cell-based therapeutics and bio-processing. The device division is operated through the Company’s ThermoGenesis subsidiary. Net Loss per Share Net loss per share is computed by dividing the net loss by the weighted average number of common shares outstanding. The calculation of the basic and diluted earnings per share is the same for all periods presented, as the effect of the potential common stock equivalents is anti-dilutive due to the Company’s net loss position for all periods presented. Anti-dilutive securities consisted of the following at June 30: 2018 2017 Vested Series A warrants 404,412 404,412 Unvested Series A warrants (1) 698,529 698,529 Warrants – other 13,197,267 3,725,782 Stock options 1,200,470 397,388 Restricted stock units -- 59,694 Total 15,500,678 5,285,805 ( 1 The unvested Series A warrants were subject to vesting based upon the amount of funds actually received by the Company in the second August 2015 February 2021. |