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Terminology used in the instructions for use for ophthalmic implants, surgical tools & instruments, OVDs, ophthalmic irrigating fluids

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Created by: Leoneska

Number of Blossarys: 1

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Packaging is the science, art and technology of enclosing or protecting products for distribution, storage, sale, and use. Packaging also refers to the process of design, evaluation, and production of packages. Packaging can be described as a coordinated system of preparing goods for transport, warehousing, logistics, sale, and end use. Packaging contains, protects, preserves, transports, informs, and sells. In many countries it is fully integrated into government, business, institutional, industrial, and personal use.

Domain: Biotechnology; Health care; Life Sciences; Medical; Medical devices; Regulatory; Category: 

confezione also: presentazione

Domain: Biotechnology; Health care; Life Sciences; Medical; Medical devices; Regulatory; Category: 

intraoculaire lens (IOL) implantaatlens kunstlens Een intraoculaire lens (IOL), ook wel implantaatlens of kunstlens genoemd, is een in het menselijk oog geïmplanteerde kunstlens, die gewoonlijk de oorspronkelijke lens vervangt omdat deze troebel is geworden ten gevolge van een cataract, of die deze lens aanvult om sterke lensafwijkingen te corrigeren. Hij bestaat gewoonlijk uit een lensje van kunststof, met twee plastic armpjes om hem binnen het lenskapsel op zijn plaats te houden. Oorspronkelijk werden IOL’s gemaakt van niet-flexibel materiaal (polymethylmethacrylaat (PMMA), ook bekend onder handelsnamen als Perspex, Plexiglas, e.d.), maar tegenwoordig worden er meer flexibele materialen voor gebruikt. De meeste IOL’s hebben een vaste sterkte, geschikt voor veraf zien. Maar er zijn ook IOL’s met meerdere sterktes, bijv. voor veraf zien én voor lezen. Ook zijn accommoderende IOL’s in ontwikkeling, waarmee men tot op zekere hoogte kan scherpstellen, vergelijkbaar met de oorspronkelijke ooglens.

Domain: Biotechnology; Health care; Life Sciences; Medical; Medical devices; Regulatory; Category: Implants & interventional materials

lente intraoculare (IOL) Una volta asportato il cristallino catarattoso sarà necessario impiantare un cosiddetto cristallino artificiale o IOL. Tale cristallino non ha però le caratteristiche di quello naturale di poter cambiare il suo spessore permettendo quindi sia la visione del lontano che del vicino, ma soltanto di una delle due distanze. Per tale motivo nella maggioranza dei casi esso si calcola per poter svolgere la vita di relazione e cioè per la lontananza; per la lettura saranno necessarie delle lenti ausiliarie (lenti da presbiopia). Il calcolo della “gradazione” del cristallino viene fatto con uno strumento chiamato ECOBIOMETRO contestualmente alla visita specialistica. Tale apparecchio permette di misurare, grazie agli ultrasuoni, la lunghezza dell’occhio e quindi stabilire la “potenza” del cristallino da impiantare.

Domain: Biotechnology; Health care; Life Sciences; Medical; Medical devices; Regulatory; Category: Implants & interventional materials

Beschrijving een verklaring voorleggen iets in woorden, van werkwoord beschrijven

Domain: Biotechnology; Health care; Life Sciences; Medical; Medical devices; Regulatory; Category: Biochemistry; Biofuel; Biomedical; Behavioral science; Cancer treatment; Dentistry; Diseases; Hematology; Hospitals; Medical research; Nursing homes; Psychiatry; Vaccines; Regulatory; Herbal medicine; Histology; Medicine; Cardiac supplies; Clinical analytical instruments; Clinical trials; Dental equipment; Dermatology instruments; Emergency room apparatus; ENT instruments; Eye instruments; General assay & diagnostic instruments; Implants & interventional materials; Medical cryogenic equipment; OBGYN equipment; Orthopaedic supplies; Pharmacology instruments; Physical therapy equipment; Radiology equipment; Sterilization equipment; Surgical instruments; Ultrasonic & optical equipment; Ward nursing equipment

Descrizione una dichiarazione che presenta qualcosa in parole, dal verbo descrivere

Domain: Biotechnology; Health care; Life Sciences; Medical; Medical devices; Regulatory; Category: Biochemistry; Biofuel; Biomedical; Behavioral science; Cancer treatment; Dentistry; Diseases; Hematology; Hospitals; Medical research; Nursing homes; Psychiatry; Vaccines; Regulatory; Herbal medicine; Histology; Medicine; Cardiac supplies; Clinical analytical instruments; Clinical trials; Dental equipment; Dermatology instruments; Emergency room apparatus; ENT instruments; Eye instruments; General assay & diagnostic instruments; Implants & interventional materials; Medical cryogenic equipment; OBGYN equipment; Orthopaedic supplies; Pharmacology instruments; Physical therapy equipment; Radiology equipment; Sterilization equipment; Surgical instruments; Ultrasonic & optical equipment; Ward nursing equipment

gebruiksaanwijzing

Domain: Biotechnology; Health care; Life Sciences; Medical; Medical devices; Regulatory; Category: Biochemistry; Biofuel; Biomedical; Behavioral science; Cancer treatment; Dentistry; Diseases; Hematology; Hospitals; Medical research; Nursing homes; Psychiatry; Vaccines; Regulatory; Herbal medicine; Histology; Medicine; Cardiac supplies; Clinical analytical instruments; Clinical trials; Dental equipment; Dermatology instruments; Emergency room apparatus; ENT instruments; Eye instruments; General assay & diagnostic instruments; Implants & interventional materials; Medical cryogenic equipment; OBGYN equipment; Orthopaedic supplies; Pharmacology instruments; Physical therapy equipment; Radiology equipment; Sterilization equipment; Surgical instruments; Ultrasonic & optical equipment; Ward nursing equipment

"a manual usually accompanying a technical device and explaining how to install or operate it" Essential Requirements - Medical Device Directive 93/42/EEC - Annex I, 13.1: Each device must be accompanied by the information needed to use it safely and to identify the manufacturer, taking account of the training and knowledge of the potential user. This information comprises the details on the label and the data in the instructions for use. As far as practicable and appropriate, the information needed to use the device safely must be set out on the device itself and/or on the packaging of each unit. If not practicable, the information must be set out in the leaflet supplied with one or more devices. Instructions for use must be included in the packaging for every device. By way of exception, no such instruction leaflet is needed for devices in Class I or Class IIa if they can be used completely safely without any such instructions.

Domain: Biotechnology; Health care; Life Sciences; Medical; Medical devices; Regulatory; Category: Biochemistry; Biofuel; Biomedical; Behavioral science; Cancer treatment; Dentistry; Diseases; Hematology; Hospitals; Medical research; Nursing homes; Psychiatry; Vaccines; Regulatory; Herbal medicine; Histology; Medicine; Cardiac supplies; Clinical analytical instruments; Clinical trials; Dental equipment; Dermatology instruments; Emergency room apparatus; ENT instruments; Eye instruments; General assay & diagnostic instruments; Implants & interventional materials; Medical cryogenic equipment; OBGYN equipment; Orthopaedic supplies; Pharmacology instruments; Physical therapy equipment; Radiology equipment; Sterilization equipment; Surgical instruments; Ultrasonic & optical equipment; Ward nursing equipment

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