Regulation of Medical Devices

Regulation of Medical Devices PDF Author: United States. Congress. House. Committee on Government Operations. Intergovernmental Relations Subcommittee
Publisher:
ISBN:
Category : Intrauterine contraceptives
Languages : en
Pages : 666

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Regulation of Medical Devices (Intrauterine Contraceptive Devices)

Regulation of Medical Devices (Intrauterine Contraceptive Devices) PDF Author: United States. Congress. House. Government Operations
Publisher:
ISBN:
Category :
Languages : en
Pages : 598

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Regulation of Medical Devices

Regulation of Medical Devices PDF Author: United States. Congress. House. Committee on Government Operations. Intergovernmental Relations Subcommittee
Publisher:
ISBN:
Category : Intrauterine contraceptives
Languages : en
Pages : 0

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Regulation of Medical Devices (Intrauterine Contraceptive Devices) - Hearings, 93Rd Congress, 1St Session, 1973

Regulation of Medical Devices (Intrauterine Contraceptive Devices) - Hearings, 93Rd Congress, 1St Session, 1973 PDF Author: United States. Congress. House. Committee on Government Operations
Publisher:
ISBN:
Category :
Languages : en
Pages : 200

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Second Report on Intrauterine Contraceptive Devices

Second Report on Intrauterine Contraceptive Devices PDF Author: Elizabeth B. Connell
Publisher:
ISBN:
Category : Intrauterine contraceptives
Languages : en
Pages : 126

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Regulation of Medical Devices (intrauterine Contraceptive Devices)

Regulation of Medical Devices (intrauterine Contraceptive Devices) PDF Author: United States. Congress. House. Committee on Government Operations
Publisher:
ISBN:
Category : Intrauterine contraceptives
Languages : en
Pages : 576

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Regulation of Medical Devices (intrauterine Contraceptive Devices).

Regulation of Medical Devices (intrauterine Contraceptive Devices). PDF Author: United States. Congress. House. Committee on Government Operations
Publisher:
ISBN:
Category :
Languages : en
Pages : 576

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Second report on intrauterine contraceptive devices

Second report on intrauterine contraceptive devices PDF Author: United States. Food and Drug Administration. Medical Device Advisory Committee on Obstetrics and Gynecology
Publisher:
ISBN:
Category :
Languages : en
Pages : 124

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Intrauterine Devices and Their Complications

Intrauterine Devices and Their Complications PDF Author: David A. Edelman
Publisher: Springer Science & Business Media
ISBN: 9401507244
Category : Medical
Languages : en
Pages : 279

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Book Description
In Memoriam xiii Preface xvii Chapter 1 Development, Mechanisms of Action and Evaluation of IUD Performance 2 Chapter 2 IUD Insertion 28 Chapter 3 Uterine Perforation 54 Chapter 4 Pelvic Inflammatory Disease 92 Chapter 5 Bleeding 138 Chapter 6 Cervical and Uterine Pathology 158 Chapter 7 Intrauterine Pregnancy 172 Chapter 8 Ectopic Pregnancy 194 Chapter 9 Return to Fertility after IUD Discontinuation 222 Chapter 10 IUD Complications in Perspective 232 Appendices 243 Index 253 Foreword Ever since Hippocrates observed that foreign bodies placed in the uterus would help to prevent pregnan cy, periodic interest in this information and its use has resulted in attempts to control unwanted fertil ity. Prior to the 1900s, this interest was somewhat episodic. Because of anxiety about infection, early attempts flourished only briefly and then were no more. In the twentieth century, however, as a result of renewed interest in intrauterine contraception, particularly in the developing countries, a number of individuals throughout the world began experiment ing with a variety of new intrauterine devices. Since then, a great number of these devices have been studied; a few have survived careful scrutiny, and IUDs now represent the second most commonly used form of medical contraception. It is estimated that approximately 15 million devices are in use at the present time, 3 to 4 million of them in the United States.

Medical Device Regulations

Medical Device Regulations PDF Author: Michael Cheng
Publisher: World Health Organization
ISBN: 9241546182
Category : Medical
Languages : en
Pages : 54

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Book Description
The term 'medical devices' covers a wide range of equipment essential for patient care at every level of the health service, whether at the bedside, at a health clinic or in a large specialised hospital. Yet many countries lack access to high-quality devices, particularly in developing countries where health technology assessments are rare and there is a lack of regulatory controls to prevent the use of substandard devices. This publication provides a guidance framework for countries wishing to create or modify their own regulatory systems for medical devices, based on best practice experience in other countries. Issues highlighted include: the need for harmonised regulations; and the adoption, where appropriate, of device approvals of advanced regulatory systems to avoid an unnecessary drain on scarce resources. These approaches allow emphasis to be placed on locally-assessed needs, including vendor and device registration, training and surveillance and information exchange systems.