Difference between revisions of "Book:Introduction to Implants, Volume 2"
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==''Introduction to Implants: Devices, Procedures, and Conditions Requiring Them'' (Volume 2) == | ==''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. [[:Book:Introduction to Implants, Volume 1|Volume 1]] included articles on what a medical device and an implant are, types of implants, | This is the second of two volumes on the topic of implantable medical devices. [[:Book:Introduction to Implants, Volume 1|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 | ;5. Implant-related Medical Conditions | ||
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:[[Organ dysfunction]] | :[[Organ dysfunction]] | ||
:[[Osteoarthritis]] | :[[Osteoarthritis]] | ||
:[[Otitis media]] | |||
:[[Otosclerosis]] | :[[Otosclerosis]] | ||
:[[Paraplegia]] | :[[Paraplegia]] | ||
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:[[Biocompatibility]] | :[[Biocompatibility]] | ||
:[[Biofunctionalization]] | |||
:[[Capsular contracture]] | :[[Capsular contracture]] | ||
:[[Cell encapsulation]] | :[[Cell encapsulation]] | ||
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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
- Biocompatibility
- Biofunctionalization
- Capsular contracture
- Cell encapsulation
- 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 logistics
- Metallic microlattice
- Microextrusion
- Minusheet perfusion culture system
- Package testing
- Polymer solution casting
- Reliability engineering
- Safety engineering
- Sintering
- 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
- Ministry of Food and Drug Safety
- Notified body
- Pharmaceuticals and Medical Devices Agency
- Postmarketing surveillance
- QSIT
- Regulation of therapeutic goods
- Regulatory affairs
- Safe Medical Device Amendments of 1990
- 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.
