N/A

GUDID 00840682140935

ASSY SECOND FRAME

GE MEDICAL SYSTEMS INFORMATION TECHNOLOGIES, INC.

Patient monitoring system module rack
Primary Device ID00840682140935
NIH Device Record Keyf9915dac-fd26-481e-9efd-55e004460e43
Commercial Distribution StatusIn Commercial Distribution
Brand NameN/A
Version Model NumberB1X5-F2
Company DUNS006580799
Company NameGE MEDICAL SYSTEMS INFORMATION TECHNOLOGIES, INC.
Device Count1
DM Exemptfalse
Pre-market Exemptfalse
MRI Safety StatusMR Unsafe
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usefalse
Lot Batchfalse
Serial Numberfalse
Manufacturing Datetrue
Expiration Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Customer Support Contacts

Phone+1(999)999-9999
Emailxx@xx.xx
Phone+1(999)999-9999
Emailxx@xx.xx
Phone+1(999)999-9999
Emailxx@xx.xx
Phone+1(999)999-9999
Emailxx@xx.xx
Phone+1(999)999-9999
Emailxx@xx.xx
Phone+1(999)999-9999
Emailxx@xx.xx
Phone+1(999)999-9999
Emailxx@xx.xx
Phone+1(999)999-9999
Emailxx@xx.xx
Phone+1(999)999-9999
Emailxx@xx.xx
Phone+1(999)999-9999
Emailxx@xx.xx
Phone+1(999)999-9999
Emailxx@xx.xx
Phone+1(999)999-9999
Emailxx@xx.xx
Phone+1(999)999-9999
Emailxx@xx.xx
Phone+1(999)999-9999
Emailxx@xx.xx
Phone+1(999)999-9999
Emailxx@xx.xx
Phone+1(999)999-9999
Emailxx@xx.xx
Phone+1(999)999-9999
Emailxx@xx.xx
Phone+1(999)999-9999
Emailxx@xx.xx
Phone+1(999)999-9999
Emailxx@xx.xx
Phone+1(999)999-9999
Emailxx@xx.xx
Phone+1(999)999-9999
Emailxx@xx.xx
Phone+1(999)999-9999
Emailxx@xx.xx
Phone+1(999)999-9999
Emailxx@xx.xx
Phone+1(999)999-9999
Emailxx@xx.xx
Phone+1(999)999-9999
Emailxx@xx.xx
Phone+1(999)999-9999
Emailxx@xx.xx
Phone+1(999)999-9999
Emailxx@xx.xx
Phone+1(999)999-9999
Emailxx@xx.xx
Phone+1(999)999-9999
Emailxx@xx.xx
Phone+1(999)999-9999
Emailxx@xx.xx
Phone+1(999)999-9999
Emailxx@xx.xx
Phone+1(999)999-9999
Emailxx@xx.xx
Phone+1(999)999-9999
Emailxx@xx.xx

Device Identifiers

Device Issuing AgencyDevice ID
GS100840682140935 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

MHXMONITOR, PHYSIOLOGICAL, PATIENT(WITH ARRHYTHMIA DETECTION OR ALARMS)

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number2
Public Version Date2021-03-01
Device Publish Date2020-11-16

On-Brand Devices [N/A]

00840682104500420915-025
00840682124348B105 Patient Monitor
00840682124331B125 Patient Monitor
008406821180952017099-001
00840682122610420915-050
00840682122597420915-004
00840682122573420915-038
00840682122566420915-089
00840682122559420915-016
00840682122542420915-042
00840682122535420915-023
00840682122528420915-011
00840682122511420915-084
00840682122504420915-069
00840682122498420915-022
00840682122481420915-002
00840682122474420915-041
00840682122467420915-049
00840682122450420915-036
008406821181562017099-003
008406821180642023807-002
00840682105408Unity Network ID
008406821052172012196-001
008406821048692017098-005
008406821048522017098-001
008406821048452017098-003
008406821048142017098-007
00840682104784Patient Data Module
00840682104777420915-080
00840682104760420915-063
00840682104753420915-031
00840682104746420915-043
00840682104722420915-093
00840682104715420915-024
00840682104708420915-001
00840682104692420915-092
00840682104685420915-070
00840682104678420915-028
00840682104661420915-033
00840682104654420915-040
00840682104647420915-060
00840682104630420915-013
00840682104623420915-082
00840682104616420915-097
00840682104609420915-052
00840682104593420915-098
00840682104586420915-077
00840682104579420915-056
00840682104562420915-091
00840682104555420915-027

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