GE LOGIQ V1 User Manual

Device Labels
LOGIQ V2/LOGIQ V1 – User Guide 4-37
Direction 5610736-100 Rev. 9
INMETRO Certification: TUV
Rheinland Brazil
Rating plate
Note: Only after Brazilian
regulatory registration is
complete, this label will be
located on the console.
“Eurasian Conformity” mark;
thesingle conformity mark
forcirculation of products on
themarkets of member-states
ofCustoms Union.
This product passed allconformity
assessment(approval)
procedures thatcorrespond to the
requirementsof applicable
technicalregulations of the
CustomsUnion.
Bottom.
This machine should be used in
compliance with law. Some
jurisdictions restrict certain uses,
such as gender determination.
Bottom of the system
Note: For China, Korea and
India only
Every system has a unique
marking for identification, the
Unique Device Identification
(UDI) Label. The UDI label
consists of a series of
alpha-numeric characters and
barcode which uniquely identify
the LOGIQ V2/LOGIQ V1 system
as a medical device
manufactured by General
Electric. Scan or enter the UDI
information into the patient health
record as required by
country-specific laws.
Rating plate
Table 4-6: Label Icons (Continued)
Label/Icon Purpose/Meaning Location

GE LOGIQ V1 Specifications

General

Brand	GE
Model	LOGIQ V1
Category	Medical Equipment
Language	English