ABMD Share Price

Open 124.82 Change Price %
High 125.55 1 Day -0.21 -0.17
Low 124.07 1 Week 1.58 1.28
Close 125.05 1 Month 7.08 6.00
Volume 345099 1 Year 31.94 34.30
52 Week High 132.95
52 Week Low 92.03
ABMD Important Levels
Resistance 2 126.42
Resistance 1 125.86
Pivot 124.89
Support 1 124.24
Support 2 123.68
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ABIOMED, Inc. (NASDAQ: ABMD)

ABMD Technical Analysis 5
As on 28th Mar 2017 ABMD Share Price closed @ 125.05 and we RECOMMEND Strong Buy for LONG-TERM with Stoploss of 113.61 & Strong Buy for SHORT-TERM with Stoploss of 115.52 we also expect STOCK to react on Following IMPORTANT LEVELS.
ABMD Target for March
1st Target up-side 126.31
2nd Target up-side 132.16
3rd Target up-side 138.01
1st Target down-side 109.63
2nd Target down-side 103.78
3rd Target down-side 97.93
ABMD Other Details
Segment EQ
Market Capital 527299872.00
Sector Healthcare
Industry Medical Appliances & Equipment
Offical website http://www.abiomed.com
ABMD Address
ABMD
22 Cherry Hill Drive
Danvers, MA 01923
United States
Phone: 978-646-1400
Fax: 978-777-8411
ABMD Latest News
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ABMD Business Profile
ABIOMED, Inc., incorporated on June 4, 1987, is a provider of mechanical circulatory support devices and offers a continuum of care to heart failure patients. The Company develops, manufacture and market products that is designed to enable the heart to rest, heal and recover by improving blood flow and/or performing the pumping function of the heart. The Company's products are used in the cardiac catheterization lab (cath lab) by interventional cardiologists and in the heart surgery suite by heart surgeons for patients who are in need of hemodynamic support prophylactically or emergently before, during or after angioplasty or heart surgery procedures. In September 2012, the Company announced that its Impella CP product received 510(k) clearance from the U.S. Food and Drug Administration (FDA) for partial circulatory support for up to six hours. In November 2012, the Company announced that the Impella RP received Investigational Device Exemption, or IDE, approval from the FDA for use in RECOVER RIGHT, a pivotal clinical study in the U.S. In December 2012, as part of the FDA's 515 Program Initiative, an FDA panel voted to recommend continuation of Class III status for temporary ventricular support devices within the non-roller type cardiopulmonary bypass blood pumps category, which includes the Company's Impella products. The Company Headquarters is at 22 Cherry Hill Drive, Danvers, Massachusetts 01923.