3M Attest 1492V Manual De Instrucciones página 6

Storage
• Best stored in the original box under normal room conditions: 59-86ºF (15-30ºC), 35-60% relative humidity (RH).
• Do not store 1492V BIs near sterilants or other chemicals.
Disposal
Dispose of used 1492V BIs according to your health care facility policy. You may wish to steam sterilize any positive biological indicators at 132°C (270°F) for 4 minutes or at
275°F (135°C) for 3 minutes in a dynamic-air-removal steam sterilizer prior to disposal.
For further information, please contact your local 3M representative or contact us at 3M.com and select your country.
Symbol Glossary
Symbol Title
Manufacturer
Date of Manufacture
Use-by date
Batch code
Catalogue number
Do not re-use
Caution
Steam indicator
British Standards Institution
(BSI) Kitemark™
For more information see, HCBGregulatory.3M.com
Symbol Description and Reference
Indicates the medical device manufacturer as defined in Medical Device Regulation (EU) 2017/745 formerly EU Directive
93/42/EEC. Source: ISO 15223, 5.1.1
Indicates the date when the medical device was manufactured. Source: ISO 15223, 5.1.3
Indicates the date after which the medical device is not to be used. Source: ISO 15223, 5.1.4
Indicates the manufacturer's batch code so that the batch or lot can be identified. Source : ISO 15223, 5.1.5
Indicates the manufacturer's catalogue number so that the medical device can be identified. Source : ISO 15223, 5.1.6
Indicates a medical device that is intended for one use or for use on a single patient during a single procedure. Source: ISO
15223, 5.4.2
Indicates the need for the user to consult the instructions for use for important cautionary information such as warnings and
precautions that cannot, for a variety of reasons, be presented on the medical device itself. Source: ISO 15223, 5.4.4
Indicates product is designed for use with steam sterilization processes. Source: ISO 11140-1, 5.6
British Standards Institution (BSI) Kitemark™ License for compliance with BS EN ISO 11138-1:2017 and BS EN ISO
11138-3:2017
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