Difference between revisions of "Book:Introduction to Implants, Volume 2"

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;6. Implant-related Terminology
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:[[Adverse event]]
:[[Biocompatibility]]
:[[Biocompatibility]]
:[[Biofilm]]
:[[Biofunctionalization]]
:[[Biofunctionalization]]
:[[Capsular contracture]]
:[[Capsular contracture]]
:[[Cell encapsulation]]
:[[Cell encapsulation]]
:[[Chemistry of biofilm prevention]]
:[[Heart nanotechnology]]
:[[Heart nanotechnology]]
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:[[Medicines and Healthcare Products Regulatory Agency]]
:[[Medicines and Healthcare Products Regulatory Agency]]
:[[Medsafe]]
:[[Medsafe]]
:[[MedWatch]]
:[[Ministry of Food and Drug Safety]]
:[[Ministry of Food and Drug Safety]]
:[[Notified body]]
:[[Notified body]]
:[[Office of Global Regulatory Operations and Policy]]
:[[Pharmaceuticals and Medical Devices Agency]]
:[[Pharmaceuticals and Medical Devices Agency]]
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:''Publications''
:''Publications and awards''
:''[[Expert Review of Medical Devices]]''
:''[[Expert Review of Medical Devices]]''
:''[[Journal of Medical Marketing]]''
:''[[Journal of Medical Marketing]]''
:''[[MD&DI]]''
:''[[MD&DI]]''
:''[[Medical & Biological Engineering & Computing]]''
:''[[Medical & Biological Engineering & Computing]]''
:[[Medical Design Excellence Awards]]


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[[Category:LIMSwiki books on healthcare]]
[[Category:LIMSwiki books on healthcare]]

Revision as of 21:00, 7 April 2016

Introduction to Implants:
Devices, Procedures, and Conditions Requiring Them (Volume 2)
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Introduction to Implants: Devices, Procedures, and Conditions Requiring Them (Volume 2)

This is the second of two volumes on the topic of implantable medical devices. Volume 1 included articles on what a medical device and an implant are, types of implants, the biomaterials used in the manufacture or implants, and medical procedures utilizing them.. This volume continues on with articles about medical conditions necessitating or caused by an implant, implant terminology, regulatory information, and implant-related resources.

5. Implant-related Medical Conditions
Adhesion (medicine)
Aneurysm
Ascites
Atrial septal defect
Bone fracture
Bradycardia
Breast cancer
Cancer
Cataract
Chronic pain
Diabetes mellitus
Disfigurement
Dystrophic calcification
Epilepsy
Erectile dysfunction
Fecal incontinence
Gastroesophageal reflux disease
Gastroparesis
Glaucoma
Hearing loss
Heart failure
Hydrocephalus
Hypertrophic cardiomyopathy
Keratoconus
Laryngeal cancer
Metallosis
Obesity
Organ dysfunction
Osteoarthritis
Otitis media
Otosclerosis
Paraplegia
Parkinson's disease
Pulmonary embolism
Respiratory failure
Retinitis pigmentosa
Rheumatoid arthritis
Scoliosis
Sinusitis
Sleep apnea
Spinal stenosis
Spondylolisthesis
Syncope (medicine)
Treatment-resistant depression
Unintended pregnancy
Urinary incontinence
Urinary retention
Valvular heart disease
Ventricular fibrillation
Ventricular septal defect
Ventricular tachycardia
Visual impairment
6. Implant-related Terminology
Adverse event
Biocompatibility
Biofilm
Biofunctionalization
Capsular contracture
Cell encapsulation
Chemistry of biofilm prevention
Heart nanotechnology
Implant failure
Nanotopography
Neuromechanics of orthoses
Neurotechnology
Osseointegration
Pacemaker failure
Staphylococcus epidermidis
Surface chemistry of neural implants
Surface and bulk erosion
Manufacturing and Distribution
3D bioprinting
3D printing
Bioburden testing
Biomedical engineering
Direct metal laser sintering
Electron beam additive manufacturing
Lattice structure
Medical device manufacturing
Medical logistics
Metallic microlattice
Microextrusion
Minusheet perfusion culture system
Package testing
Polymer solution casting
Reliability engineering
Safety engineering
Sintering
Software reliability testing
Stereolithography
Sterility assurance level
7. Regulatory Considerations
21 CFR Part 11
Center for Devices and Radiological Health
Central Drugs Standard Control Organization
China Food and Drug Administration
Design controls
Design history file
Federal Food, Drug, and Cosmetic Act
Food and Drug Administration Amendments Act of 2007
Food and Drug Administration Modernization Act of 1997
Food and Drug Administration
Global Harmonization Task Force
Global Medical Device Nomenclature
Humanitarian Device Exemption
IEC 60601
IEC 62304
IEC 62366
ISO 10993
ISO 13485
ISO 14155
ISO 14971
ISO/IEEE 11073
ISO/TC 215
Italian Device Registration
Medical Device Radiocommunications Service
Medical Device Regulation Act
Medical device reporting
Medical Devices Directive
Medicines and Healthcare Products Regulatory Agency
Medsafe
MedWatch
Ministry of Food and Drug Safety
Notified body
Office of Global Regulatory Operations and Policy
Pharmaceuticals and Medical Devices Agency
Postmarketing surveillance
QSIT
Regulation of therapeutic goods
Regulatory affairs
Safe Medical Device Amendments of 1990
Software of unknown pedigree
Therapeutic Goods Administration
Therapeutic Products Directorate
Type approval
8. Resources
Manufacturers
Abbott Laboratories, Inc.
Abiomed, Inc.
Alcon, Inc.
Allergan, Plc
Bausch & Lomb, Inc.
Bayer AG
Berlin Heart GmbH
Biotronik SE & Co. KG
Boston Scientific Corporation
DePuy Synthes, Inc.
Glaukos Corporation
Intersect ENT, Inc.
Medtronic PLC
Mentor Worldwide, LLC
MetaCure Ltd.
Navilyst Medical, Inc.
Novartis International AG
Smith & Nephew PLC
St. Jude Medical, Inc.
Stryker Corporation
SynCardia Systems, Inc.
Teva Pharmaceutical Industries Ltd.
Zimmer Biomet Holdings, Inc.
Organizations
AdvaMed
American Society for Artificial Internal Organs
Association for the Advancement of Medical Instrumentation
Canadian Medical and Biological Engineering Society
COCIR
Cyborg Foundation
MedTech Europe
Publications and awards
Expert Review of Medical Devices
Journal of Medical Marketing
MD&DI
Medical & Biological Engineering & Computing
Medical Design Excellence Awards