In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 3: In vitro diagnostic instruments for professional use
Also Known As:
SKU148151895
Published by
Deutsches Institut für Normung
DIN
Publication Date2013-01
Pages CountPages19
This part of DIN EN ISO 18113 specifies requirements for information supplied by the manufacturer of IVD instruments for professional use. Furthermore, this part of DIN EN ISO 18113 also applies to apparatus and equipment intended to be used with IVD instruments for professional use. This part of DIN EN ISO 18113 can also be applied to accessories, where appropriate.
Details
| Descriptors | Apparatus for analysis, Applications, CE marking, Data of the manufacturer, Diagnosis, Diagnostic equipment, Diagnostic systems, Enterprises, Experts, Handling, In vitro, Information, Information supplied by the manufacturer, Installations, Instructions for use, Instruments, Investigations, In-vitro diagnostic, Labelling, Laboratory medicine, Medical equipment, Medical products, Medical sciences, Medical technology, Occupational safety, Operational instructions, Personnel, Product information, Specification (approval), User information, Workplace safety, Medical devices, Implementation, Diagnosis (medical), Use |
| ICS Codes | 11.100.10 - In vitro diagnostic test systems |
| Language(s) | English |
| File Size | 409.6 KB |
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