WARNING

Indicates the need for the user to consult the instructions for use for important cautionary

CONSULT INSTRUCTIONS FOR USE

Indicates the need for the user to consult the instructions for use

MANUFACTURER

Indicates the medical device manufacturer, as defined in EU Directives 90/385/EEC, 93/42/EEC and 98/79/EC

DATE OF MANUFACTURE

Indicates the date when the medical device was manufactured.

SERIAL NUMBER

Indicates the manufacturer’s serial number so that a specific medical device can be identified.

CATALOGUE NUMBER

Indicates the manufacturer’s catalogue number so that the medical device can be identified

MAX USER WEIGHT

Indicates the maximun userweight of the device

SEAT WIDTH

Indicates the seat width of the of the device

PART NUMBER CHASSIS

Indicates the part number for the chassis of the wheelchair

PART NUMBER CHASSIS

Indicates the part number for the chassis of the wheelchair. Rev. 2

PART NUMBER LABEL AND REVISION

Indicates the part number for the label and what revision

MEDICAL DEVICE

Indicates that the device is a medical device as defined in MDR 2017/745-

CE MARK
Indicates manufacturer declaration that the product complies with the essential/ general safety & performance requirements of the relevant European medical device, health, safety and environmental protection legislations.

NO PASSENGER SEAT

Indicates that the product must not be used as a passanger seat in a vehicle transport

PRESCRIPTION DEVICE

Indicates that the product is a medical device as defined in 21 CFR 820.3(l) and Federal Law (USA) restricts this device to sale by or on the order of a physician.