Indicates the manufacturer’s batch code so that the batch or lot can be identified.
ISO 15223-1:2021 Medical devices – Symbols to be used with medical device labels, labelling and information to be supplied – Part 1: General requirements.
Symbols glossary
Mölnlycke Health Care’s labelling is designed to meet all applicable international standards and regulations. Where possible, Mölnlycke Health Care adopted the use of symbols to communicate requirements, product characteristics and provide guidance on handling and storage to the user. A compiled listing of symbols that may appear on the product labelling and the meaning of the symbol is provided in this document.
Batch code (LOT)
Catalogue number (REF)
Indicates the manufacturer’s catalogue number so that the medical device can be identified.
ISO 15223-1:2021 Medical devices – Symbols to be used with medical device labels, labelling and information to be supplied – Part 1: General requirements.
Caution, see instructions for use
ISO 15223-1:2021 Medical devices – Symbols to be used with medical device labels, labelling and information to be supplied – Part 1: General requirements.
Caution: Federal (USA) Law restricts this device to sale by or on the order of a physician (or properly licensed practitioner) (Rx only)
21 CFR 801.109
Contains or presence of natural rubber latex
Indicates the presence of dry natural rubber or natural rubber latex as a material of construction within the medical device or the packaging of a medical device
ISO 15223-1:2021 Medical devices – Symbols to be used with medical device labels, labelling and information to be supplied – Part 1: General requirements.
Consult instructions for use
Indicates the need for the user to consult the instructions for use
ISO 15223-1:2021 Medical devices – Symbols to be used with medical device labels, labelling and information to be supplied – Part 1: General requirements.
No presence of natural rubber latex
Expiry date
Indicates the date after which the medical device is not to be used
ISO 15223-1:2021 Medical devices – Symbols to be used with medical device labels, labelling and information to be supplied – Part 1: General requirements.
Medical device (MD)
Indicates the item is a medical device
ISO 15223-1:2021 Medical devices – Symbols to be used with medical device labels, labelling and information to be supplied – Part 1: General requirements.
Serial number (SN)
Indicates the manufacturer’s serial number so that a specific medical device can be identified
ISO 15223-1:2021 Medical devices – Symbols to be used with medical device labels, labelling and information to be supplied – Part 1: General requirements.
Unique Device Identifier (UDI)
Indicates a carrier that contains unique device identifier information
ISO 15223-1:2021 Medical devices – Symbols to be used with medical device labels, labelling and information to be supplied – Part 1: General requirements.
Date of manufacture
ISO 15223-1:2021 Medical devices – Symbols to be used with medical device labels, labelling and information to be supplied – Part 1: General requirements.
Single patient – multiple use
ISO 15223-1:2021 Medical devices – Symbols to be used with medical device labels, labelling and information to be supplied – Part 1: General requirements.
Product information-Wound care
Can be cut
Product information-Wound care
Highly exuding wounds
Product information-Wound care
Moderately exuding wounds
Product information-Wound care
Low exuding wounds
Product information-Wound care
Shower proof
Product information-Wound care
Wound pad size and product area
Product information-Wound care
Wound pad size and product area
Product information-Wound care
Wound pad size and product area
Product information-Wound care
Wound pad size and product area
Product information-Wound care
Wound pad size and product area
Product information – Avance System
BF applied part To identify a type BF applied part complying with IEC 60601-1.
IEC 60601-1, Medical electrical equipment — Part 1: General requirements for basic safety and essential performance.
Product information – Avance System
Caution related to batteries
Product information – Avance System
Class II equipment to identify equipment meeting the safety requirements specified for Class II equipment.
IEC 60601-1, Medical electrical equipment — Part 1: General requirements for basic safety and essential performance.
Product information – Avance System
Follow instructions for use.
IEC 60601-1:2005/ COR1:2006 Medical electrical equipment — Part 1: General requirements for basic safety and essential performance. Table D.2, Symbol 10.
Product information – Avance System
Indicates air leakage in a Negative Pressure Wound Therapy system.
Product information – Avance System
Indicates blockage in a Negative Pressure Wound Therapy system.
Product information – Avance System
Indicates low battery.
Product information – Avance System
Indoor use to identify electrical equipment designed primarily for indoor use.
IEC 60417 Graphical Symbols for Use on Equipment.
Product information – Avance System (IP22)
Ingress Protection.
Product information – Avance System
MR unsafe
ASTM F2503 Standard Practice for Marking Medical Devices and Other Items for Safety in the Magnetic Resonance Environment.
Product information – Avance System
Recycle: Electronic Equipment.
Marking of electrical and electronic equipment in accordance with Article 11(2) of Directive 2002/96/EC (WEEE).
Product information – Avance System
System lasts up to 14 days.
Product information - Turning & Positioners
Body weight
Product information - Turning & Positioners
First day in use
Product information - Turning & Positioners
MR safe
ASTM F2503 Standard Practice for Marking Medical Devices and Other Items for Safety in the Magnetic Resonance Environment.
Product information - Turning & Positioners
Patient number Indicates a unique number associated with an individual patient
ISO 15223-1:2021 Medical devices – Symbols to be used with medical device labels, labelling and information to be supplied – Part 1: General requirements.
Product information - Turning & Positioners
Wipe off
Product information - Turning & Positioners
Write
Do not bleach
ISO 3758:2012 Textiles -- Care labelling code using symbols
Do not dry clean
ISO 3758:2012 Textiles -- Care labelling code using symbols
Do not iron
ISO 3758:2012 Textiles -- Care labelling code using symbols
Do not tumble dry
ISO 3758:2012 Textiles -- Care labelling code using symbols
Do not wash
ISO 3758:2012 Textiles -- Care labelling code using symbols
Iron
Iron at maximum sole-plate temperature of 110°C without steam
Washing at 30°C
Maximum washing temperature 30°C in normal condition
Washing at 60°C
Maximum washing temperature 60°C in normal condition
Tumble drying possible
ISO 3758:2012 Textiles -- Care labelling code using symbols
Wash by hand
Maximum temperature by 40ºC
ISO 3758:2012 Textiles -- Care labelling code using symbols
Corrosive
Flammable
Globally Harmonized System of Classification and Labelling of Chemicals (GHS)
Hazardous to environment
Globally Harmonized System of Classification and Labelling of Chemicals (GHS)
Health Hazard/Hazardous to Ozone layer
Globally Harmonized System of Classification and Labelling of Chemicals (GHS)
Sterility steam or dry heat
Indicates a medical device that has been sterilised using steam or dry heat
ISO 15223-1:2021 Medical devices – Symbols to be used with medical device labels, labelling and information to be supplied – Part 1: General requirements.
Sterile
Indicates a medical device that has been subjected to a sterilisation process
ISO 15223-1:2021 Medical devices – Symbols to be used with medical device labels, labelling and information to be supplied – Part 1: General requirements.
Sterility ETO
Indicates a medical device that has been sterilised using ethylene oxide
ISO 15223-1:2021 Medical devices – Symbols to be used with medical device labels, labelling and information to be supplied – Part 1: General requirements.
Sterility irradiation
Indicates a medical device that has been sterilised using irradiation
ISO 15223-1:2021 Medical devices – Symbols to be used with medical device labels, labelling and information to be supplied – Part 1: General requirements.
Single sterile barrier system
Indicates a single sterile barrier system
ISO 15223-1:2021 Medical devices – Symbols to be used with medical device labels, labelling and information to be supplied – Part 1: General requirements.
Single sterile barrier system with protective packaging inside
Indicates a single sterile barrier system with protective packaging inside
ISO 15223-1:2021 Medical devices – Symbols to be used with medical device labels, labelling and information to be supplied – Part 1: General requirements.
Do not re-use
Indicates a medical device that is intended for one single use only
ISO 15223-1:2021 Medical devices – Symbols to be used with medical device labels, labelling and information to be supplied – Part 1: General requirements.
Do not use if package is damaged
Indicates that a medical device that should not be used if the package has been damaged or opened and that the user should consult the instructions for use for additional information
ISO 15223-1:2021 Medical devices – Symbols to be used with medical device labels, labelling and information to be supplied – Part 1: General requirements.
Non-sterile
Indicates a medical device that has not been subjected to a sterilisation process
ISO 15223-1:2021 Medical devices – Symbols to be used with medical device labels, labelling and information to be supplied – Part 1: General requirements.
CE-mark
CE-mark with Notified Body identification number
UKCA-mark with Approved body identification number
UK Conformity mark
Authorised Representative (EC REP)
CH REP/ Swiss Authorised Representative & Importer
Distributor
Indicates the entity distributing the medical device into the locale
ISO 15223-1:2021 Medical devices – Symbols to be used with medical device labels, labelling and information to be supplied – Part 1: General requirements.
Manufacturer
Indicates the medical device manufacturer
ISO 15223-1:2021 Medical devices – Symbols to be used with medical device labels, labelling and information to be supplied – Part 1: General requirements.
Importer
Indicates the entity importing the medical device into the locale
ISO 15223-1:2021 Medical devices – Symbols to be used with medical device labels, labelling and information to be supplied – Part 1: General requirements.
Humidity limitation
Indicates the range of humidity to which the medical device can be safely exposed
ISO 15223-1:2021 Medical devices – Symbols to be used with medical device labels, labelling and information to be supplied – Part 1: General requirements.
Atmospheric pressure limitation
Indicates the range of atmospheric pressure to which the medical device can be safely exposed
ISO 15223-1:2021 Medical devices – Symbols to be used with medical device labels, labelling and information to be supplied – Part 1: General requirements.
Keep away from sunlight
Indicates a medical device that needs protection from light sources
ISO 15223-1:2021 Medical devices – Symbols to be used with medical device labels, labelling and information to be supplied – Part 1: General requirements.
Keep dry
Indicates a medical device that needs to be protected from moisture
ISO 15223-1:2021 Medical devices – Symbols to be used with medical device labels, labelling and information to be supplied – Part 1: General requirements.
Temperature limit
Indicates the temperature limits to which the medical device can be safely exposed
ISO 15223-1:2021 Medical devices – Symbols to be used with medical device labels, labelling and information to be supplied – Part 1: General requirements.
Lower limit of temperature
Indicates the lower limit of temperature to which the medical device can be safely exposed
ISO 15223-1:2021 Medical devices – Symbols to be used with medical device labels, labelling and information to be supplied – Part 1: General requirements.
Upper limit of temperature
Indicates the upper limit of temperature to which the medical device can be safely exposed
ISO 15223-1:2021 Medical devices – Symbols to be used with medical device labels, labelling and information to be supplied – Part 1: General requirements.
Do not use box cutter
This way up
ISO 7000 Graphical symbols for use on equipment — Registered symbols.
Green dot symbol
Packaging recovery organisation Europe
Recycling symbol
ISO 7001 Graphical symbols -- Public information symbols. Ref. no: PI PF 066
QR code
QR Code leading to my.molnlycke.com
Triman logo – French waste directive
Product information – EasyWarm
Fixation belts, tape, straps or supplemental bedding must not be used on top of the blanket. Do not tuck blanket under patient's arms, legs or body and do not place the blanket under the patient. The anaesthetized patient's arms, legs and limbs must not be placed on top of blanket
Product information – EasyWarm
Monitor cutaneous response regularly, according to clinical judgment. When accessing the patient, turn or slide the blanket and do not fold the blanket over itself.
Product information – EasyWarm
Do not fold the blanket over itself.
Product information – EasyWarm
The blanket must not be used on patients with severe impairment to peripheral (including skin) circulation.
Product information – EasyWarm
The warming pads must be facing up, away from the patient. Correct side indicated by “THIS SIDE UP” marking on the blanket.
The warming pads must be facing up, with the white side of the blanket towards the patient. Correct side indicated by “THIS SIDE UP” marking on the blanket.
Product information – EasyWarm, REF 629905
Surgery on hands, arms and head, place the blanket over the entire body.
Product information – EasyWarm, REF 629905
Upper body/thoracic surgery, place the blanket over the lower part of the body.
Product information – EasyWarm, REF 629905
Surgery on lower body and/or extremities, place the blanket over arms and chest.
Product information – EasyWarm, REF 629915
Surgery on hands, arms and head, place the blanket over the entire body.
Product information – EasyWarm, REF 629915
Upper body/thoracic surgery, split the blanket and place the lower parts over legs and hips. The upper part may be placed over arms and chest.
Product information – EasyWarm, REF 629915
Surgery on lower body and/or extremities, split the blanket and place the upper part over arms and chest.
Product information – EasyWarm, REF 629915
Surgery in the abdominal area, split the blanket and place the upper part over arms and chest and place the lower parts over legs and hips.
Definitions and Symbols are reproduced from standards with due permission from the Swedish Institute for Standards (www.sis.se), Tel: +46 (0)8 555 523 10) which is the owner and copyright holder of the standards.
