cobas h 232 User Manual

5
On the packaging and on the identification plate of the meter you may encounter the following symbols,
shown here with their meaning:
On meters with WLAN capability:
For other WLAN certifications, see label on bottom of battery compartment and addendum for
information on WLAN registration.
The user is fully responsible for the installation, use and upkeep of the cobas h 232 meter.
Caution, consult accompanying documents. Refer to safety-related notes in the
instructions for use accompanying this instrument.
Temperature limitation (Store at)
Manufacturer
Catalogue number
In vitro diagnostic medical device
Global Trade Item Number
This product fulfills the requirements of the European Directives 98/79/EC on in
vitro diagnostic medical devices and 1999/5/EC on radio and telecommunications
terminal equipment (R&TTE).
The system fulfills the Canadian and U.S. safety requirements (UL LISTED, in
accordance with UL 61010A-1:02 and CAN/CSA-C22.2 No.61010-1-04).
This device complies with Part 15 of the FCC Rules and with RSS-210 of Industry
Canada
IVD

cobas h 232 Specifications

General

Device Type	Point-of-care analyzer
Sample Type	Whole blood, plasma
Measured Parameters	Troponin T, Myoglobin, D-Dimer, NT-proBNP
Connectivity	USB
Intended Use	cardiac markers
Data Management	LIS connectivity
Throughput	Single test
Sample Volume	150 µL
Operating Temperature	15-30 °C
Operating Humidity	10-85% (non-condensing)
Display	Color touchscreen
Measurement Principle	Electrochemiluminescence immunoassay (ECLIA)