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Showing 1 to 12 of 93 entries
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Medical device and laboratory product problem reporting program (PRP).

FDA drug bulletin

[No authors listed]
PMID: 510843
FDA Drug Bull. 1979 Nov;9(5):30.

No abstract available.

FDA's medical device standards policy.

Journal of parenteral science and technology : a publication of the Parenteral Drug Association

Stimson RA.
PMID: 7229834
J Parenter Sci Technol. 1981 Mar-Apr;35(2):60-2.

No abstract available.

Emergency use of unapproved medical devices.

FDA drug bulletin

[No authors listed]
PMID: 4092901
FDA Drug Bull. 1985 Dec;15(4):36-7.

No abstract available.

Appliances go to market via the FDA. 1.

ET journal

Koch MJ.
PMID: 255404
ET J. 1979;6(1):27-9. doi: 10.1097/00152192-197900610-00008.

No abstract available.

Recognizing outstanding achievements in health care.

Ostomy/wound management

[No authors listed]
PMID: 1580974
Ostomy Wound Manage. 1992 Apr;38(3):54, 56-7.

No abstract available.

[Congress 86. Strong desire for influence on new technology].

Sygeplejersken

[No authors listed]
PMID: 3638013
Sygeplejersken. 1986 Jul 02;86(27):13.

No abstract available.

Broad new quality standards for the manufacture of medical devices.

Public health reports (Washington, D.C. : 1974)

[No authors listed]
PMID: 715166
Public Health Rep. 1978 Nov-Dec;93(6):679.

No abstract available.

[Study of Chinese medical device standardization situation and development strategy].

Zhongguo yi liao qi xie za zhi = Chinese journal of medical instrumentation

Tian X, Xu H, Peng X.
PMID: 24195398
Zhongguo Yi Liao Qi Xie Za Zhi. 2013 Jul;37(4):285-6.

Based on the analysis of Chinese medical device standardization situation, providing recommendations for the development strategy of Chinese medical device standardization proceed from the duty and advantage of standardized participation.

[Analysis on the main difference and impact between IEC 60601-1 in Ed. 3.1 and GB 9706.1-2007].

Zhongguo yi liao qi xie za zhi = Chinese journal of medical instrumentation

Zheng J, He J, Yu X.
PMID: 25980136
Zhongguo Yi Liao Qi Xie Za Zhi. 2014 Nov;38(6):442-4.

For the preparation of implementing IEC 60601-1 Ed. 3.1 in advance, this paper analyzes the main difference between IEC 60601-1 Ed. 3.1 and GB 9706.1-2007, and discusses the possible influence to medical device designing and testing.

[Understanding and Thinking on America Clinical Evaluation of Medical Devices].

Zhongguo yi liao qi xie za zhi = Chinese journal of medical instrumentation

Yuan F, Yuan P, Deng G.
PMID: 26904887
Zhongguo Yi Liao Qi Xie Za Zhi. 2015 Sep;39(5):372-5, 387.

This paper introduces the risk classification and listing way of medical devices in the United States, and according to the contents in various situations, FDA provides the requirements for clinical evaluation. At the same time, through the comparative study...

A bleak future for new drugs and devices.

Tennessee nurse

Porterfield L.
PMID: 8399262
Tenn Nurse. 1993;56(2):9.

No abstract available.

FDA's performance standard for electrode lead wires and patient cables. Second phase is now being implemented.

Health devices

[No authors listed]
PMID: 11002440
Health Devices. 2000 Apr;29(4):140-1.

No abstract available.

Showing 1 to 12 of 93 entries