Cardiac Device Safety.
- Published in:
- JAMA: Journal of the American Medical Association, 2005, v. 294, n. 20, p. 2564, doi. 10.1001/jama.294.20.2564-a
- By:
- Publication type:
- Article
Works matching DE "PRODUCT liability -- Medical instruments %26 apparatus"
Results: 29
1
2
Surveillance of Medical Device–Related Hazards and Adverse Events in Hospitalized Patients.
- Published in:
- JAMA: Journal of the American Medical Association, 2004, v. 291, n. 3, p. 325, doi. 10.1001/jama.291.3.325
- By:
- Publication type:
- Article
3
Critical assessment of new devices.
- Published in:
- Perfusion, 2007, v. 22, n. 3, p. 167, doi. 10.1177/0267659107076877
- By:
- Publication type:
- Article
4
Standards update on perfusion equipment and practice.
- Published in:
- Perfusion, 2005, v. 20, n. 4, p. 205, doi. 10.1191/0267659105pf808oa
- By:
- Publication type:
- Article
5
Normen: Grundlegende Anforderungen an Medizinprodukte im Rahmen der Medizinprodukteverordnung (MDR).
- Published in:
- Quintessenz der Zahntechnik, 2021, v. 47, n. 10, p. 1200
- By:
- Publication type:
- Article
6
A French approach to cost-effectiveness analysis?
- Published in:
- 2010
- By:
- Publication type:
- Editorial
7
PATIENTS OVER POLITICS: ADDRESSING LEGISLATIVE FAILURE IN THE REGULATION OF MEDICAL PRODUCTS.
- Published in:
- Wisconsin Law Review, 2011, v. 2011, n. 5, p. 929
- By:
- Publication type:
- Article
8
NicOx announces Phase IIa results for PF-03187207.
- Published in:
- Expert Review of Ophthalmology, 2008, v. 3, n. 3, p. 258
- By:
- Publication type:
- Article
9
Product liability floodgates haven't been opened.
- Published in:
- Urology Times, 1996, v. 24, n. 8, p. 2
- By:
- Publication type:
- Article
10
How Technology is Shifting Agency from Doctors to Patients: The Cost and Impact of Medical Technologies to Traditional Liability and Malpractice.
- Published in:
- Journal of Corporation Law, 2019, v. 44, n. 3, p. 609
- By:
- Publication type:
- Article
11
Medical Device Regulations and Testing for Toxicologic Pathologists.
- Published in:
- Toxicologic Pathology, 2008, v. 36, n. 1, p. 63, doi. 10.1177/0192623307309926
- By:
- Publication type:
- Article
12
Recall of A&A medical devices.
- Published in:
- Contemporary OB/GYN, 2002, v. 47, n. 6, p. 26
- Publication type:
- Article
13
Pacemaker Malfunction Simulated by Amplifier Saturation.
- Published in:
- Pacing & Clinical Electrophysiology, 1985, v. 8, n. 5, p. 757, doi. 10.1111/j.1540-8159.1985.tb05889.x
- By:
- Publication type:
- Article
14
Reversible EOL-Indicator: A New Cause for Low Pacemaker Rate.
- Published in:
- Pacing & Clinical Electrophysiology, 1983, v. 6, n. 3, p. 680, doi. 10.1111/j.1540-8159.1983.tb05325.x
- By:
- Publication type:
- Article
15
Publications Update.
- Published in:
- 2016
- Publication type:
- journal article
16
The Fidelis Recall: How Much Pressure Can the ICD World Bear?
- Published in:
- 2008
- By:
- Publication type:
- Editorial
17
Impact of Fusion Avoidance on Performance of the Automatic Threshold Tracking Feature in Dual Chamber Pacemakers: A Multicenter Prospective Randomized Study.
- Published in:
- Pacing & Clinical Electrophysiology, 2002, v. 25, n. 11, p. 1540, doi. 10.1046/j.1460-9592.2002.01540.x
- By:
- Publication type:
- Article
18
Present Day Pacemakers for Pulse Generator Exchange: Is 3.5 V a Sufficient Nominal Setting for the Pulse Amplitude?
- Published in:
- Pacing & Clinical Electrophysiology, 1996, v. 19, n. 11, p. 1824
- By:
- Publication type:
- Article
19
FDA requires health care facilities to report death and injury from medical devices.
- Published in:
- Public Health Reports, 1992, v. 107, n. 2, p. 238
- Publication type:
- Article
20
Closed-loop verification of medical devices with model abstraction and refinement.
- Published in:
- International Journal on Software Tools for Technology Transfer, 2014, v. 16, n. 2, p. 191, doi. 10.1007/s10009-013-0289-7
- By:
- Publication type:
- Article
21
Washington Supreme Court Holds that Medical Device Manufacturers Have a Duty to Warn Hospitals - Taylor v. Intuitive Surgical, Inc.
- Published in:
- American Journal of Law & Medicine, 2017, v. 43, n. 1, p. 165, doi. 10.1177/0098858817718163
- By:
- Publication type:
- Article
22
A reply.
- Published in:
- 2007
- By:
- Publication type:
- Letter
23
Potentially confusing markings on a tracheal tube.
- Published in:
- 2007
- By:
- Publication type:
- Letter
24
CASE REPORT Disruption of cleft palate repair following the use of the laryngeal mask airway.
- Published in:
- Anaesthesia, 2004, v. 59, n. 4, p. 401, doi. 10.1111/j.1365-2044.2004.03662.x
- By:
- Publication type:
- Article
25
Oversight of medical device safety and effectiveness remains inadequate.
- Published in:
- Canadian Medical Association Journal (CMAJ), 2011, v. 183, n. 10, p. E651
- By:
- Publication type:
- Article
26
HUMAN ERROR: IS IT AN INEVITATBLE PART OF HEALTH CARE, OR IS THERE A BETTER FUTURE?
- Published in:
- RT: The Journal for Respiratory Care Practitioners, 2008, v. 21, n. 3, p. 24
- By:
- Publication type:
- Article
27
Shaping Up China's Medical Device Industry.
- Published in:
- China Business Review, 2008, v. 35, n. 3, p. 24
- By:
- Publication type:
- Article
28
Characterizing and configuring motorized wedge for a new generation telecobalt machine in a treatment planning system.
- Published in:
- Journal of Medical Physics, 2007, v. 32, n. 1, p. 29, doi. 10.4103/0971-6203.31147
- By:
- Publication type:
- Article
29
Direct-to-consumer genetic testing -- a regulatory nightmare?
- Published in:
- Medical Journal of Australia, 2013, v. 198, n. 9, p. 501, doi. 10.5694/mja12.10350
- By:
- Publication type:
- Article