INSTRUCTIONS FOR USE
Symbols:
Symbol used
Indicates the device is a medical device
Indicates the medical device manufacturer
Indicates the manufacturer's serial number
Indicates the medical device Global Trade Item Number
Indicates the manufacturer's lot code
Indicates the date when the medical device was manufactured
Indicates the manufacturer's catalogue number
Indicates the need for the user to consult the instructions for use
for important cautionary information such as warnings and
precautions.
Indicates the device do not contain natural rubber or dry natural
rubber latex
Indicates the authorized representative in the European
Community
Indicates the Medical Device complies to REGULATION (EU)
2017/745
Indicates a Warning
Indicates the need for the user to consult the instruction for use
Property of Kyra Medical, Inc. ©2021
Description
Page 3
Reference
MDR 2017/745
EN ISO 15223-1
EN ISO 15223-1
21 CFR 830
MDR 2017/745
EN ISO 15223-1
EN ISO 15223-1
EN ISO 15223-1
EN ISO 15223-1
EN ISO 15223-1
EN ISO 15223-1
MDR 2017/745
IEC 60601-1
EN ISO 15223-1
IFU Document Number: 03-0370-REV-F