UNI - Medical Collection
This collection contains documents from the following standards organization(s): Ente Nazionale Italiano di Unificazione
| UNI UNI EN ISO 10524-4 | EN-Pressure regulators for use with medical gases - Part 4: Low-pressure regulators | |
| UNI UNI EN ISO 10535 | EN-Hoists for the transfer of disabled persons - Requirements and test methods | |
| UNI UNI EN ISO 10535 | EN-Hoists for the transfer of disabled persons - Requirements and test methods | |
| UNI UNI EN ISO 10535 | EN-Hoists for the transfer of disabled persons - Requirements and test methods | |
| UNI UNI EN ISO 10555-1 | EN-Sterile single-use intravascular catheters - General requirements | |
| UNI UNI EN ISO 10555-1 | EN-Sterile single-use intravascular catheters - Part 1: General requirements | |
| UNI UNI EN ISO 10555-1 | EN-Sterile single-use intravascular catheters - Part 1: General requirements | |
| UNI UNI EN ISO 10555-1 | EN-Sterile single-use intravascular catheters - General requirements | |
| UNI UNI EN ISO 10555-2 | EN-Sterile single-use intravascular catheters - Angiographic catheters. | |
| UNI UNI EN ISO 10555-3 | EN-Sterile single-use intravascular catheters - Central venous catheters | |
| UNI UNI EN ISO 10555-4 | EN-Sterile single-use intravascular catheters - Balloon dilatation catheters | |
| UNI UNI EN ISO 10555-5 | EN-Sterile single-use intravascular catheters - Over-needle peripheral catheters | |
| UNI UNI EN ISO 10555-5 | EN-Sterile single-use intravascular catheters - Over-needle peripheral catheters. | |
| UNI UNI EN ISO 10637 | EN-Dental equipment - High- and medium- volume suction systems | |
| UNI UNI EN ISO 10650-1 | EN-Dentistry - Powered polymerization activators - Part 1: Quartz tungsten halogen lamps | |
| UNI UNI EN ISO 10650-2 | EN-Dentistry - Powered polymerization activators - Part 2: Light-emitting diode (LED) lamps | |
| UNI UNI EN ISO 10651-2 | EN-Lung ventilators for medical use - Particular requirements for basic safety and essential performance - Part 2: Home care ventilators for ventilator- dependent patients | |
| UNI UNI EN ISO 10651-2 | EN-Lung ventilators for medical use - Particular requirements for basic safety and essential performance - Part 2: Home care ventilators for ventilator- dependent patients | |
| UNI UNI EN ISO 10651-4 | EN-Lung ventilators - Particular requirements for operator-powered resuscitators | |
| UNI UNI EN ISO 10651-4 | EN-Lung ventilators - Part 4: Particular requirements for operator-powered resuscitators | |
| UNI UNI EN ISO 10651-6 | EN-Lung ventilators for medical use - Particular requirements for basic safety and essential performance - Part 6: Home-care ventilatory support devices | |
| UNI UNI EN ISO 10651-6 | EN-Lung ventilators for medical use - Particular requirements for basic safety and essential performance - Part 6: Home-care ventilatory support devices | |
| UNI UNI EN ISO 10938 | EN-Ophthalmic instruments - Chart projectors. | |
| UNI UNI EN ISO 10939 | EN-Ophthalmic instruments - Slit-lamp microscopes | |
| UNI UNI EN ISO 10939 | EN-Ophthalmic instruments - Slit-lamp microscopes | |
| UNI UNI EN ISO 10940 | EN-Ophthalmic instruments - Fundus cameras | |
| UNI UNI EN ISO 10940 | EN-Ophthalmic instruments - Fundus cameras | |
| UNI UNI EN ISO 10942 | EN-Ophthalmic instruments - Direct ophthalmoscopes. | |
| UNI UNI EN ISO 10942 | EN-Ophthalmic instruments - Direct ophthalmoscopes | |
| UNI UNI EN ISO 10943 | EN-Ophthalmic instruments - Indirect ophthalmoscopes | |
| UNI UNI EN ISO 10943 | EN-Ophthalmic instruments - Indirect ophthalmoscopes. | |
| UNI UNI EN ISO 10944 | EN-Ophthalmic instruments - Synoptophores | |
| UNI UNI EN ISO 10944 | EN-Ophthalmic instruments - Synoptophores | |
| UNI UNI EN ISO 10993-1 | EN-Biological evaluation of medical devices - Part 1: Evaluation and testing | |
| UNI UNI EN ISO 10993-1 | EN-Biological evaluation of medical devices - Evaluation and testing | |
| UNI UNI EN ISO 10993-1 | EN-Biological evaluation of medical devices - Part 1: Evaluation and testing within a risk management process | |
| UNI UNI EN ISO 10993-1 | EN-Biological evaluation of medical devices - Part 1: Evaluation and testing | |
| UNI UNI EN ISO 10993-10 | EN-Biological evaluation of medical devices - Part 10: Tests for irritation and delayed-type hypersensitivity | |
| UNI UNI EN ISO 10993-10 | EN-Biological evaluation of medical devices. Tests of irritation and sensitization. | |
| UNI UNI EN ISO 10993-10 | EN-Biological evaluation of medical devices - Part 10: Tests for irritation and delayed-type hypersensitivity | |
| UNI UNI EN ISO 10993-11 | EN-Biological evaluation of medical devices. Tests for systemic toxicity. | |
| UNI UNI EN ISO 10993-11 | EN-Biological evaluation of medical devices - Part 11: Tests for systemic toxicity | |
| UNI UNI EN ISO 10993-11 | EN-Biological evaluation of medical devices - Part 11: Tests for systemic toxicity | |
| UNI UNI EN ISO 10993-11 | EN-Biological evaluation of medical devices - Part 11: Tests for systemic toxicity | |
| UNI UNI EN ISO 10993-12 | EN-Biological evaluation of medical devices - Part 12: Sample preparation and reference materials | |
| UNI UNI EN ISO 10993-12 | EN-Biological evaluation of medical devices - Part 12: Sample preparation and reference materials | |
| UNI UNI EN ISO 10993-12 | EN-Biological evaluation of medical devices - Part 12: Sample preparation and reference materials | |
| UNI UNI EN ISO 10993-12 | EN-Biological evaluation of medical devices - Part 12: Sample preparation and reference materials | |
| UNI UNI EN ISO 10993-12 | EN-Biological evaluation of medical devices - Sample preparation and reference materials. | |
| UNI UNI EN ISO 10993-12 | EN-Biological evaluation of medical devices - Part 12: Sample preparation and reference materials | |
| UNI UNI EN ISO 10993-13 | EN-Biological evaluation of medical devices - Part 13: Identification and quantification of degradation products from polymeric medical devices | |
| UNI UNI EN ISO 10993-13 | EN-Biological evaluation of medical devices - Identification and quantification of degradation products from polymeric medical devices | |
| UNI UNI EN ISO 10993-13 | EN-Biological evaluation of medical devices - Part 13: Identification and quantification of degradation products from polymeric medical devices | |
| UNI UNI EN ISO 10993-14 | EN-Biological evaluation of medical devices - Identification and quantification of degradation products from ceramics | |
| UNI UNI EN ISO 10993-14 | EN-Biological evaluation of medical devices - Part 14: Identification and quantification of degradation products from ceramics | |
| UNI UNI EN ISO 10993-15 | EN-Biological evaluation of medical devices - Part 15: Identification and quantification of degradation products from metals and alloys | |
| UNI UNI EN ISO 10993-15 | EN-Biological evaluation of medical devices - Identification and quantification of degradation products from metals and alloys | |
| UNI UNI EN ISO 10993-16 | EN-Biological evaluation of medical devices - Part 16: Toxicokinetic study design for degradation products and leachables | |
| UNI UNI EN ISO 10993-16 | EN-Biological evaluation of medical devices - Part 16: Toxicokinetic study design for degradation products and leachables | |
| UNI UNI EN ISO 10993-16 | EN-Biological evaluation of medical devices - Toxicokinetic study design for degradation products and leachables . | |
| UNI UNI EN ISO 10993-17 | EN-Biological evaluation of medical devices - Part 17: Establishment of allowable limits for leachable substances | |
| UNI UNI EN ISO 10993-17 | EN-Biological evaluation of medical devices - Part 17: Establishment of allowable limits for leachable substances | |
| UNI UNI EN ISO 10993-18 | EN-Biological evaluation of medical devices - Part 18: Chemical characterization of materials | |
| UNI UNI EN ISO 10993-18 | EN-Biological evaluation of medical devices - Part 18: Chemical characterization of materials | |
| UNI UNI EN ISO 10993-2 | EN-Biological evaluation of medical devices - Part 2: Animal welfare requirements | |
| UNI UNI EN ISO 10993-2 | EN-Biological evaluation of medical devices - Part 2: Animal welfare requirements | |
| UNI UNI EN ISO 10993-2 | EN-Biological evaluation of medical devices - Animal welfare requirements | |
| UNI UNI EN ISO 10993-3 | EN-Biological evaluation of medical devices - Part 3: Tests for genotoxicity carcinogenicity and reproductive toxicity | |
| UNI UNI EN ISO 10993-3 | EN-Biological evaluation of medical devices - Part 3: Tests for genotoxicity carcinogenicity and reproductive toxicity | |
| UNI UNI EN ISO 10993-4 | EN-Biological evaluation of medical devices - Part 4: Selection of tests for interactions with blood | |
| UNI UNI EN ISO 10993-4 | EN-Biological evaluation of medical devices - Part 4: Selection of tests for interactions with blood | |
| UNI UNI EN ISO 10993-4 | EN-Biological evaluation of medical devices - Selection of tests for interactions with blood | |
| UNI UNI EN ISO 10993-5 | EN-Biological evaluation of medical devices - Part 5: Tests for in vitro cytotoxicity | |
| UNI UNI EN ISO 10993-5 | EN-Biological evaluation of medical devices - Tests for in vitro cytotoxicity | |
| UNI UNI EN ISO 10993-6 | EN-Biological evaluation of medical devices - Part 6: Tests for local effects after implantation | |
| UNI UNI EN ISO 10993-6 | EN-Biological evaluation of medical devices - Part 6: Tests for local effects after implantation | |
| UNI UNI EN ISO 10993-7 | EN-Biological evaluation of medical devices. Ethylene oxide sterilization residuals. | |
| UNI UNI EN ISO 10993-7 | EN-Biological evaluation of medical devices - Part 7: Ethylene oxide sterilization residuals | |
| UNI UNI EN ISO 10993-8 | EN-Biological evaluation of medical devices - Selection and qualification of reference materials for biological tests |