K-TEK KTEK9000 Instructions For Use Manual page 4

INSTRUCTIONS FOR USE
2.4 Symbols:
Symbol Used
©2023 Kyra Medical, Inc.
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 instruc-
tions 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 authorized representative in
Switzerland
Indicates the authorized representative in the
United Kingdom
Indicates the Medical Device complies to REGULA-
TION UK MDR 2002
Indicates the Medical Device complies to REGULA-
TION (EU) 2017/745
Indicates a Warning
Indicates the need for the user to consult the instruc-
tion for use
Description
4
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
EN ISO 15223-1
EN ISO 15223-1
UK MDR 2002
MDR 2017/745
IEC 60601-1
EN ISO 15223-1
IFU 03-0235 REV J