DEVICE: NA (00840682146708)
Device Identifier (DI) Information
NA
B105 VSP3.0 Patient Monitor
In Commercial Distribution
6160000-003
GE MEDICAL SYSTEMS INFORMATION TECHNOLOGIES, INC.
B105 VSP3.0 Patient Monitor
In Commercial Distribution
6160000-003
GE MEDICAL SYSTEMS INFORMATION TECHNOLOGIES, INC.
B105M ATO MODEL
Device Characteristics
MR Unsafe | |
No | |
No | |
No | |
No | |
No | |
No | |
No | |
No |
GMDN
[?]GMDN© Term Code, Names and Definitions (*Terms of Use): GMDN® is a registered trademark of The GMDN Agency. All rights reserved. Used under licence from The GMDN Agency Ltd.
GMDN Term Code | GMDN Term Name | GMDN Term Definition | GMDN Term Status [?] | Implantable? |
---|---|---|---|---|
33586 | General-purpose multi-parameter bedside monitor |
An electrically-powered device/device assembly designed for the continuous assessment of several vital physiologic parameters (e.g., ECG, blood pressure, heart rate, temperature, cardiac output, apnoea, and respiratory/anaesthetic gas concentrations) of one patient in intensive or general healthcare settings. It typically set-up by the patient bedside and often includes programmable alarms, portable radio transmitters, receivers, and antennas (telemetry systems) to allow monitoring during patient ambulation or transportation; it is not dedicated to neonatal use and is not intended to be worn on the body.
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Active | false |
FDA Product Code
[?]Product Code | Product Code Name |
---|---|
FLL | Thermometer, electronic, clinical |
OLT | Non-normalizing quantitative electroencephalograph software |
CCL | ANALYZER, GAS, OXYGEN, GASEOUS-PHASE |
DSJ | Alarm, blood-pressure |
CBS | ANALYZER, GAS, HALOTHANE, GASEOUS-PHASE (ANESTHETIC CONC.) |
CCK | ANALYZER, GAS, CARBON-DIOXIDE, GASEOUS-PHASE |
DPZ | Oximeter, ear |
OLW | Index-generating electroencephalograph software |
DXN | System, measurement, blood-pressure, non-invasive |
CBQ | ANALYZER, GAS, ENFLURANE, GASEOUS-PHASE (ANESTHETIC CONCENTRATION) |
DQA | Oximeter |
BZQ | Monitor, breathing frequency |
ORT | Burst suppression detection software for electroencephalograph |
GWQ | Full-montage Standard Electroencephalograph |
NHO | Analyzer, gas, desflurane, gaseous-phase (anesthetic concentration) |
MHX | MONITOR, PHYSIOLOGICAL, PATIENT(WITH ARRHYTHMIA DETECTION OR ALARMS) |
NHP | Analyzer, gas, sevoflurane, gaseous-phase (anesthetic concentration) |
KRB | PROBE, THERMODILUTION |
CBR | ANALYZER, GAS, NITROUS-OXIDE, GASEOUS PHASE (ANESTHETIC CONC.) |
OMC | Reduced- montage standard electroencephalograph |
DRT | MONITOR, CARDIAC (INCL. CARDIOTACHOMETER & RATE ALARM) |
NHQ | Analyzer, gas, isoflurane, gaseous-phase (anesthetic concentration) |
DSK | COMPUTER, BLOOD-PRESSURE |
MLD | MONITOR, ST SEGMENT WITH ALARM |
KOI | STIMULATOR, NERVE, PERIPHERAL, ELECTRIC |
DQK | Computer, diagnostic, programmable |
DSI | DETECTOR AND ALARM, ARRHYTHMIA |
FDA Premarket Submission
FDA Premarket Submission Number [?] | Supplement Number [?] |
---|---|
K213490 | 000 |
Sterilization
Storage and Handling
[?]Storage and Handling |
---|
Handling Environment Humidity: between 15 and 90 Percent (%) Relative Humidity |
Handling Environment Atmospheric Pressure: between 70 and 106 KiloPascal |
Handling Environment Temperature: between 5 and 35 Degrees Celsius |
Storage Environment Temperature: between -20 and 60 Degrees Celsius |
Storage Environment Humidity: between 10 and 90 Percent (%) Relative Humidity |
Storage Environment Atmospheric Pressure: between 70 and 106 KiloPascal |
Clinically Relevant Size
[?]Size Type Text |
---|
No Device Sizes |
Device Record Status
77bc6ad3-4125-48b8-9319-85a262714478
April 20, 2022
1
April 12, 2022
April 20, 2022
1
April 12, 2022
Alternative and Additional Identifiers Additional Identifiers
Package DI
[?]Package DI Number | Quantity per Package | Contains DI Package | Package Discontinue Date | Package Status | Package Type |
---|---|---|---|---|---|
No Package DIs found |
Secondary DI
[?]Issuing Agency [?] | Secondary DI Number |
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No Secondary DIs found |
Unit of Use DI
[?]
Unit of Use DI Number:
No Unit of Use DI Numbers Found
CLOSE
Direct Marking (DM)
[?]Production Identifier(s) in UDI
[?]Customer Contact
[?]
+1(999)999-9999
xx@xx.xx
xx@xx.xx