Braun ExactFit 3 Manual De Instrucciones página 15

MEDICAL ELECTRICAL EQUIPMENT needs special precautions regarding EMC.
For detailed description of EMC requirements visit www.BraunHealthcare.com.
Portable and mobile RF communications equipment can affect medical electrical equipment.
Please do not dispose of the product in the household waste at the end of its useful life. Disposal
can take place at your local retailer or at appropriate collection points provided in your country.
Warranty
Please read all instructions before attempting to use this device. Please retain the receipt as proof
of and date of purchase. The receipt must be presented when making any claim within the relevant
warranty period. Any claim under the warranty will not be valid without a proof of purchase.
Your device is warrantied for two years (2 years) from date of purchase.
This warranty covers defects in materials or workmanship that occur under normal use; defective
devices meeting these criteria will be replaced free of charge.
The warranty DOES NOT cover defects or damage resulting from abuse or failure to follow the user
instructions. The warranty becomes void if the device is opened, tampered with, or used with non-
Braun branded parts or accessories, or if repairs are undertaken by unauthorized persons.
Accessories and consumables are excluded from any warranty.
For support requests or warranty claims, please contact us by calling 1-800-327-7226 or emailing us at
ConsumerRelations@HelenofTroy.com.
The LOT and SN of your device are printed on the rating label on the back of the product.
Production date is given by the LOT located in the back of the device. The first 3 numeric digits after
the LOT No. represents the day of the year of manufacture. The next 2 numeric digits represent
the last two numbers of the calendar year of manufacture and the letters at the end designate the
manufacturer of the product. E.g. LOT 15614TRA, this product was made on day 156, year 2014, at
manufacturer identifier TRA.
This device conforms to the following standards:
• AAMI SP10:2002 - Manual, Electronic or Automated Spygmomanometers
• IEC 80601-2-30 Medical electrical equipment – Part 2-30: Particular requirements for the basic safety
and essential performance of automated non-invasive sphygmomanometers
• ANSI /AAMI/ IEC 60601-1: Medical electrical equipment – Part 1: General requirements for basic safety
and essential performance
• IEC 60601-1-2: Medical electrical equipment – Part 1-2: General requirements for basic safety and
essential performance – Collateral Standard: Electromagnetic disturbances – Requirement and tests
NOTE: DO NOT use this device in the presence of electromagnetic or other interference outside the
normal range specified in IEC 60601-1-2.
• ISO 15223-1: Medical devices - Symbols to be used with medical device labels, labeling and
information to be supplied - Part 1: General requirements
• IEC 60601-1-11: Medical electrical equipment – Part 1-11: General requirements for basic safety
and essential performance – Collateral standard: Requirements for medical electrical equipment and
medical electrical systems used in the home healthcare environment
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